Canonical Allele Identifier: PA2826562582
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 629930
ClinVar RCV Id: RCV000820689 RCV000774787 RCV002290023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Lys132Asn
CA287486593
NM_001276697.3:c.396G>C
CA397836562
NM_001276697.3:c.396G>T