Canonical Allele Identifier: PA2828029170
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 947448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gln2322Glu
CA16038305
NM_001354906.2:c.6964C>G