Allele Registry

Canonical Allele Identifier: PA2825331839

Gene: GCH1 HGNC NCBI

ClinVar RCV:

RCV002949635

ClinVar Variation:

2072725

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019195.1:p.Arg59Gly	CA7193669 NM_001024024.2:c.175C>G