ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579952368
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.3316810053
Score
-0.2510370863
Score
-0.221416502
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000456310
RCV000570325
RCV002289598
ClinVar Variation:
406587
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ser314Phe
CA001234
NM_000546.6:c.941C>T