Canonical Allele Identifier: PA2827998995
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2539Asn
CA049224
NM_001354901.2:c.7616C>A