Canonical Allele Identifier: PA658734077
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492573
ClinVar RCV Id: RCV000584249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Ser376Phe
CA397830633
NM_001126112.3:c.1127C>T