Canonical Allele Identifier: PA2579936914
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376632
ClinVar RCV Id: RCV000421931 RCV000424730 RCV000433045 RCV000433598 RCV000434970 RCV000442091 RCV000442462 RCV000443054 RCV001041362 RCV004022228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Leu111Gln
CA16603051
NM_000546.6:c.332T>A