Canonical Allele Identifier: PA2828055614
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 849086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala947Val
CA16028617
NM_001354905.2:c.2840C>T