Canonical Allele Identifier: PA095392
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 189011
ClinVar RCV Id: RCV000169398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg402Gln
CA274253
NM_000159.4:c.1205G>A