Canonical Allele Identifier: PA2825605691
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Gly302Glu
CA16615695
NM_001126113.3:c.905G>A