ClinGen Allele Registry
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Canonical Allele Identifier:
PA300205
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.1025952023
Score
-0.89401103
Score
1.3131762032
Score
0.626179766
Score
-0.5016267251
Score
-0.665048572
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000161033
RCV000200500
RCV000419726
RCV000421083
RCV000421733
RCV000422107
RCV000429307
RCV000430423
RCV000431774
RCV000434187
RCV000439317
RCV000439996
RCV000443569
RCV000443583
RCV001526334
RCV002288692
ClinVar Variation:
182934
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Met237Val
CA000348
NM_000546.6:c.709A>G