Canonical Allele Identifier: PA916041609
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2644Ser
CA16038447
NM_001354896.2:c.7930A>T
CA16038449
NM_001354896.2:c.7931C>G