Allele Registry

Canonical Allele Identifier: PA108119

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000427349

RCV000546517

ClinVar Variation:

378583

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Arg227His	CA3403949 NM_003060.4:c.680G>A