Allele Registry

Canonical Allele Identifier: PA913201614

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022339

RCV000438010

ClinVar Variation:

25386

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Thr256Met	CA342644 NM_001308122.2:c.767C>T