Canonical Allele Identifier: PA916009211
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 459947
ClinVar RCV Id: RCV000551437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Arg355His
CA9234590
NM_013976.3:c.1064G>A