Canonical Allele Identifier: PA2825619440
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492573
ClinVar RCV Id: RCV000584249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Ser337Phe
CA397830633
NM_001126118.1:c.1010C>T