ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA107338
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.6114912992
Score
-0.0087189969
Score
-0.105420592
Score
0.8666620883
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000492688
RCV002527066
RCV004023284
ClinVar Variation:
428909
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Val172Phe
CA397841576
NM_000546.6:c.514G>T