Canonical Allele Identifier: PA095553
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 188946
ClinVar RCV Id: RCV000169320
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Gly354Ser
CA274169
NM_000159.4:c.1060G>A