Canonical Allele Identifier: PA2825619049
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Asn272Ser
CA16615690
NM_001126118.1:c.815A>G