Canonical Allele Identifier: PA2828031804
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala194Thr
CA16022765
NM_001354904.2:c.580G>A