Canonical Allele Identifier: PA645436185
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406606
ClinVar RCV Id: RCV000462657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Asp52Gly
CA16615998
NM_001126117.1:c.155A>G