Canonical Allele Identifier: PA2827947937
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr2626Ser
CA16038447
NM_001354895.2:c.7876A>T
CA16038449
NM_001354895.2:c.7877C>G