Canonical Allele Identifier: PA2828005554
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Val439Ala
CA028518
NM_001354902.2:c.1316T>C