Canonical Allele Identifier: PA915978299
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 662690
ClinVar RCV Id: RCV001017117 RCV003141850 RCV003332266 RCV003389250 RCV000820398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Ala347Thr
CA397832443
NM_001126112.3:c.1039G>A