Canonical Allele Identifier: PA1139728927
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 862517
ClinVar RCV Id: RCV001069251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Asn215Asp
CA404318460
NM_013976.3:c.643A>G