Canonical Allele Identifier: PA645479870
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 377917
ClinVar RCV Id: RCV000444441 RCV000553882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg132Gln
CA16608038
NM_000159.4:c.395G>A