Canonical Allele Identifier: PA916008971
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 189150
ClinVar RCV Id: RCV000169574 RCV000255875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Arg88Cys
CA274425
NM_013976.3:c.262C>T