Canonical Allele Identifier: PA645479959
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 226416
ClinVar RCV Id: RCV000211677 RCV003235136 RCV004020587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Val276Leu
CA9234497
NM_000159.4:c.826G>T
CA404319119
NM_000159.4:c.826G>C