Canonical Allele Identifier: PA916009145
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 188872
ClinVar RCV Id: RCV000169226 RCV000480428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Arg257Trp
CA274064
NM_013976.3:c.769C>T