Canonical Allele Identifier: PA916009181
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 750633
ClinVar RCV Id: RCV000927620 RCV001547078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Gly296Ser
CA9234537
NM_013976.3:c.886G>A