Canonical Allele Identifier: PA2825613845
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1360091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Glu126Asp
CA397837660
NM_001126116.1:c.378A>T
CA397837662
NM_001126116.1:c.378A>C