Canonical Allele Identifier: PA645479964
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 430833
ClinVar RCV Id: RCV000495869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg294Pro
CA404319364
NM_000159.4:c.881G>C