Canonical Allele Identifier: PA095317
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 188872
ClinVar RCV Id: RCV000169226 RCV000480428
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg257Trp
CA274064
NM_000159.4:c.769C>T