Canonical Allele Identifier: PA916009060
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 529445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_039663.1:p.Gln160Arg
CA404317639
NM_013976.3:c.479A>G