Canonical Allele Identifier: PA916009174
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 430833
ClinVar RCV Id: RCV000495869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Arg294Pro
CA404319364
NM_013976.3:c.881G>C