Canonical Allele Identifier: PA2827968716
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp1673Gly
CA16032465
NM_001354898.2:c.5018A>G