Canonical Allele Identifier: PA2828042754
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gln1626Glu
CA16032822
NM_001354904.2:c.4876C>G