Canonical Allele Identifier: PA2828031620
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1172085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala174Gly
CA16022640
NM_001354904.2:c.521C>G