Canonical Allele Identifier: PA2827998987
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile2536Val
CA16038238
NM_001354901.2:c.7606A>G