Allele Registry

Canonical Allele Identifier: PA126198

Gene: GPT HGNC NCBI

ClinVar RCV:

RCV000017468

ClinVar Variation:

16088

HGVS (amino-acid)	Matching Registered Transcripts
NP_005300.1:p.His14Asp	CA126197 NM_005309.2:c.40C>G