Canonical Allele Identifier: PA2825598822
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1778520
ClinVar RCV Id: RCV002398859

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Asp57Val
CA397846310
NM_001126112.3:c.170A>T