Canonical Allele Identifier: PA916041985
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile993Thr
CA007931
NM_001354897.2:c.2978T>C