Canonical Allele Identifier: PA916009009
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 288248
ClinVar RCV Id: RCV000284260 RCV000671394
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Ser119Leu
CA10606016
NM_013976.3:c.356C>T