Canonical Allele Identifier: PA916009189
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 581598
ClinVar RCV Id: RCV000705476 RCV003314640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Ser305Leu
CA404319459
NM_013976.3:c.914C>T