Canonical Allele Identifier: PA2825600557
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1386154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Val217Leu
CA397839964
NM_001126112.3:c.649G>C
CA397839966
NM_001126112.3:c.649G>T