Allele Registry

Canonical Allele Identifier: PA342617

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV003615732

ClinVar Variation:

2916364

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Pro46Ala	CA342616 NM_003060.4:c.136C>G