Canonical Allele Identifier: PA2828009164
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220442
ClinVar Variation Id: 470028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp1834Glu
CA043621
NM_001354905.2:c.5502C>G
CA16034426
NM_001354905.2:c.5502C>A