Canonical Allele Identifier: PA2825070541
Gene: GCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2926692
ClinVar RCV Id: RCV003788930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000152.1:p.Ala47Val
CA389794190
NM_000161.3:c.140C>T