Allele Registry

Canonical Allele Identifier: PA2829419054

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV002003878

RCV003323969

ClinVar Variation:

1486807

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Thr232Ala	CA3403952 NM_003060.4:c.694A>G