Canonical Allele Identifier: PA2825070029
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 951653
ClinVar RCV Id: RCV001223617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg227Gln
CA9234463
NM_000159.4:c.680G>A