Canonical Allele Identifier: PA220435
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 92531
ClinVar RCV Id: RCV000078252 RCV000546348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Val143Ala
CA220434
NM_000159.4:c.428T>C