Allele Registry

Canonical Allele Identifier: PA2825070623

Gene: GCH1 HGNC NCBI

ClinVar Allele:

1177789

ClinVar RCV:

RCV001546383

RCV002568967

ClinVar Variation:

1187065

HGVS (amino-acid)	Matching Registered Transcripts
NP_000152.1:p.Ser80Asn	CA7193654 NM_000161.3:c.239G>A