Canonical Allele Identifier: PA2827990016
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2585Ser
CA16038447
NM_001354900.2:c.7753A>T
CA16038449
NM_001354900.2:c.7754C>G