Canonical Allele Identifier: PA2825070019
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1685842
ClinVar RCV Id: RCV002250009
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Val224Gly
CA404318568
NM_000159.4:c.671T>G