Allele Registry

Canonical Allele Identifier: PA915956720

Gene: GCH1 HGNC NCBI

ClinVar RCV:

RCV000481039

ClinVar Variation:

423661

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019242.1:p.Ala101Thr	CA16619875 NM_001024071.2:c.301G>A