Canonical Allele Identifier: PA658676624
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 459950
ClinVar RCV Id: RCV000539095 RCV003330762
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg94Trp
CA404315788
NM_000159.4:c.280C>T