Canonical Allele Identifier: PA1139728971
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 951653
ClinVar RCV Id: RCV001223617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Arg227Gln
CA9234463
NM_013976.3:c.680G>A