Canonical Allele Identifier: PA2828012832
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1062362
ClinVar RCV Id: RCV003771188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Glu2419Gly
CA16038130
NM_001354905.2:c.7256A>G