Canonical Allele Identifier: PA2828032628
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Met340Val
CA027319
NM_001354904.2:c.1018A>G