Canonical Allele Identifier: PA2825605695
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Ser303Asn
CA10580912
NM_001126113.3:c.908G>A