Canonical Allele Identifier: PA2826561968
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141359
ClinVar RCV Id: RCV000129849 RCV000233843 RCV000662659 RCV001552973 RCV003321512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Ser26Asn
CA000264
NM_001276697.3:c.77G>A