Canonical Allele Identifier: PA916009142
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 374435
ClinVar RCV Id: RCV000416219 RCV000674290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Ser255Leu
CA9234481
NM_013976.3:c.764C>T