Canonical Allele Identifier: PA2827981206
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181829
ClinVar RCV Id: RCV000159581 RCV000322812 RCV000525703 RCV000575937 RCV003998426 RCV002307415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys2675Glu
CA014335
NM_001354899.2:c.8023A>G