Canonical Allele Identifier: PA916009263
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2085
ClinVar RCV Id: RCV000002166 RCV000255833 RCV001813936 RCV002512670 RCV003447469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Arg402Trp
CA252097
NM_013976.3:c.1204C>T