Canonical Allele Identifier: PA220429
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 92527
ClinVar RCV Id: RCV000078248 RCV000812634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg386Pro
CA220428
NM_000159.4:c.1157G>C