Canonical Allele Identifier: PA2828029136
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys2316Asn
CA014071
NM_001354906.2:c.6948A>C
CA16038265
NM_001354906.2:c.6948A>T