Canonical Allele Identifier: PA2827996295
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1714Ile
CA16032962
NM_001354901.2:c.5141C>T