Canonical Allele Identifier: PA916009210
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 430222
ClinVar RCV Id: RCV000494375 RCV000670238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Arg355Cys
CA9234589
NM_013976.3:c.1063C>T