Canonical Allele Identifier: PA2825069652
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1313580
ClinVar RCV Id: RCV001763944
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Gln37Arg
CA9234207
NM_000159.4:c.110A>G