Canonical Allele Identifier: PA658679187
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485045
ClinVar RCV Id: RCV000573984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ala78Thr
CA397845606
NM_001126114.3:c.232G>A