Canonical Allele Identifier: PA916009077
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 371271
ClinVar RCV Id: RCV000409563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Gly178Arg
CA9234423
NM_013976.3:c.532G>A
CA404317989
NM_013976.3:c.532G>C