Canonical Allele Identifier: PA095704
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 581598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ser305Leu
CA404319459
NM_000159.4:c.914C>T