Canonical Allele Identifier: PA191274
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile983Thr
CA007931
NM_001127510.3:c.2948T>C