Canonical Allele Identifier: PA2828052609
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Met306Val
CA027319
NM_001354905.2:c.916A>G