Canonical Allele Identifier: PA297684
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_000029.2:p.Gly2058Asp
CA010991
NM_000038.6:c.6173G>A