Canonical Allele Identifier: PA916009190
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 379529
ClinVar RCV Id: RCV000421572 RCV002524845 RCV000671835
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Arg313Trp
CA9234549
NM_013976.3:c.937C>T