Canonical Allele Identifier: PA2828035962
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala801Gly
CA007779
NM_001354904.2:c.2402C>G