Canonical Allele Identifier: PA2827977812
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1707985

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val1647Gly
CA16032325
NM_001354899.2:c.4940T>G