Canonical Allele Identifier: PA658679436
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458574
ClinVar RCV Id: RCV000527123 RCV000561902 RCV000664300 RCV000986056 RCV000989706 RCV003330753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Arg306Gln
CA287486566
NM_001126114.3:c.917G>A