Canonical Allele Identifier: PA2825070170
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 967475
ClinVar RCV Id: RCV001242396 RCV002375281
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Asp318Asn
CA9234552
NM_000159.4:c.952G>A