Canonical Allele Identifier: PA2825613969
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376594
ClinVar RCV Id: RCV000418965 RCV000419602 RCV000421032 RCV000426140 RCV000429241 RCV000429016 RCV000437299 RCV000439252 RCV000438621 RCV000481465 RCV000824076 RCV002289522 RCV002289523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Phe138Ser
CA16603016
NM_001126116.1:c.413T>C