Canonical Allele Identifier: PA916009251
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 193799
ClinVar RCV Id: RCV000173983 RCV000429838
ClinVar Variation Id: 1070251
ClinVar RCV Id: RCV001382324
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Gly390Arg
CA274950
NM_013976.3:c.1168G>C
CA404321607
NM_013976.3:c.1168G>A