Canonical Allele Identifier: PA2828023921
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn1660Thr
CA10582324
NM_001354903.2:c.4979A>C