Canonical Allele Identifier: PA2827969558
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln1927Glu
CA16034137
NM_001354898.2:c.5779C>G