Canonical Allele Identifier: PA2825615936
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Gly147Arg
CA397836876
NM_001126117.1:c.439G>C
CA397836877
NM_001126117.1:c.439G>A