Canonical Allele Identifier: PA168338
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142431
ClinVar RCV Id: RCV000131548 RCV000458425 RCV000679368 RCV001030738 RCV001527096 RCV003467176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Gly108Ser
CA000114
NM_001126112.3:c.322G>A