Canonical Allele Identifier: PA916039989
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala945Gly
CA007779
NM_001354896.2:c.2834C>G