Canonical Allele Identifier: PA2825607795
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1378428
ClinVar RCV Id: RCV001881135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ala189Gly
CA397840857
NM_001126114.3:c.566C>G