Canonical Allele Identifier: PA916041996
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn998Thr
CA16028070
NM_001354899.2:c.2993A>C