Canonical Allele Identifier: PA916009111
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 430567
ClinVar RCV Id: RCV000493776 RCV000668340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Thr214Met
CA404318457
NM_013976.3:c.641C>T