Canonical Allele Identifier: PA2826560686
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1360099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Lys81Arg
CA397844347
NM_001276696.3:c.242A>G