Canonical Allele Identifier: PA2828044935
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Leu1913Phe
CA010933
NM_001354904.2:c.5739G>T
CA16034721
NM_001354904.2:c.5739G>C