Canonical Allele Identifier: PA2826559058
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 848797
ClinVar RCV Id: RCV001052628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Ala39Ser
CA397845601
NM_001276695.3:c.115G>T