Canonical Allele Identifier: PA2828016824
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala414Val
CA030702
NM_001354906.2:c.1241C>T