Canonical Allele Identifier: PA095312
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 529442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg257Gln
CA9234482
NM_000159.4:c.770G>A