Allele Registry

Canonical Allele Identifier: PA916009029

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000665802

ClinVar Variation:

550912

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Ser139Trp	CA404317502 NM_013976.3:c.416C>G