Canonical Allele Identifier: PA2828015365
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Met330Val
CA004131
NM_001354903.2:c.988A>G