Canonical Allele Identifier: PA2827998261
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1506415
ClinVar RCV Id: RCV003773379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Leu2319Ile
CA16036865
NM_001354901.2:c.6955C>A