Canonical Allele Identifier: PA2828018855
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1063950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala728Val
CA16027966
NM_001354906.2:c.2183C>T