Canonical Allele Identifier: PA168104
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ser303Gly
CA000491
NM_001126114.3:c.907A>G