Canonical Allele Identifier: PA916009176
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2081
ClinVar RCV Id: RCV000002162 RCV000724276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Tyr295His
CA252094
NM_013976.3:c.883T>C