Canonical Allele Identifier: PA2826563065
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.His20Asp
CA16603031
NM_001276698.3:c.58C>G