Canonical Allele Identifier: PA2828013136
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr2466Ser
CA16038447
NM_001354905.2:c.7396A>T
CA16038449
NM_001354905.2:c.7397C>G