Canonical Allele Identifier: PA891845886
Gene: GCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 577041
ClinVar RCV Id: RCV000699697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000152.1:p.Ser77Cys
CA7193659
NM_000161.3:c.230C>G