Canonical Allele Identifier: PA2828048659
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Glu2477Gly
CA014080
NM_001354904.2:c.7430A>G