Canonical Allele Identifier: PA658655220
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 444396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Met28Val
CA397841976
NM_001126117.1:c.82A>G