Canonical Allele Identifier: PA916009035
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 188921
ClinVar RCV Id: RCV000169288 RCV000254928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Ser139Leu
CA274128
NM_013976.3:c.416C>T