Canonical Allele Identifier: PA916041978
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met476Val
CA027319
NM_001354897.2:c.1426A>G