Canonical Allele Identifier: PA1139729184
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 967475
ClinVar RCV Id: RCV001242396 RCV002375281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Asp318Asn
CA9234552
NM_013976.3:c.952G>A