Canonical Allele Identifier: PA2827993707
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp930Gly
CA034127
NM_001354901.2:c.2789A>G