Canonical Allele Identifier: PA2828005427
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met375Val
CA027319
NM_001354902.2:c.1123A>G