Canonical Allele Identifier: PA2827969898
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181773
ClinVar RCV Id: RCV000218693 RCV000759438 RCV003650402 RCV002516404 RCV003998396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly2033Asp
CA010991
NM_001354898.2:c.6098G>A