Canonical Allele Identifier: PA2828027972
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482314
ClinVar RCV Id: RCV000575795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn2301Thr
CA16037020
NM_001354903.2:c.6902A>C