Canonical Allele Identifier: PA164483
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala927Gly
CA007779
NM_000038.6:c.2780C>G