Canonical Allele Identifier: PA2826567439
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376598
ClinVar RCV Id: RCV000420461 RCV000425222 RCV000425855 RCV000430671 RCV000435260 RCV000435460 RCV000438306 RCV000443062 RCV000443210 RCV001027160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Phe231Val
CA16603020
NM_001276761.3:c.691T>G