Canonical Allele Identifier: PA916009132
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 235475
ClinVar RCV Id: RCV000224188 RCV002516226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Gly241Glu
CA9234469
NM_013976.3:c.722G>A