Canonical Allele Identifier: PA2827959601
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys1714Thr
CA16032502
NM_001354897.2:c.5141A>C