Canonical Allele Identifier: PA2827998212
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gly2303Ala
CA16036765
NM_001354901.2:c.6908G>C