Canonical Allele Identifier: PA2828042915
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1035716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys1644Asn
CA16032941
NM_001354904.2:c.4932G>C
CA16032942
NM_001354904.2:c.4932G>T