Allele Registry

Canonical Allele Identifier: PA108419

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022339

RCV000438010

ClinVar Variation:

25386

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Thr232Met	CA342644 NM_003060.4:c.695C>T