Canonical Allele Identifier: PA2828048830
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2500Ser
CA16038447
NM_001354904.2:c.7498A>T
CA16038449
NM_001354904.2:c.7499C>G