Canonical Allele Identifier: PA095694
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 188921
ClinVar RCV Id: RCV000169288 RCV000254928
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ser139Leu
CA274128
NM_000159.4:c.416C>T