Canonical Allele Identifier: PA168691
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142552
ClinVar RCV Id: RCV000131746 RCV000195550 RCV001284721 RCV002267882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Gly228Val
CA000030
NM_001126115.1:c.683G>T