Canonical Allele Identifier: PA2828034505
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala609Val
CA007259
NM_001354904.2:c.1826C>T