Allele Registry

Canonical Allele Identifier: PA112598

Gene: G6PC1 HGNC NCBI

ClinVar Variation Id: 1988441

ClinVar RCV Id: RCV002781305

ClinVar Variation Id: 2716659

ClinVar RCV Id: RCV003513205

HGVS (amino-acid)	Matching Registered Transcripts
NP_000142.2:p.Phe322Leu	CA399657329 NM_000151.4:c.964T>C CA399657352 NM_000151.4:c.966C>A CA399657354 NM_000151.4:c.966C>G