Canonical Allele Identifier: PA891861865
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 575773
ClinVar RCV Id: RCV000698086 RCV001183319 RCV002289975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ala69Thr
CA397845904
NM_001126114.3:c.205G>A