Canonical Allele Identifier: PA916009185
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 429706
ClinVar RCV Id: RCV000494627 RCV000587206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Ala298Thr
CA9234539
NM_013976.3:c.892G>A