Allele Registry

Canonical Allele Identifier: PA2829418938

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV001216413

ClinVar Variation:

945707

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Arg169Pro	CA360804515 NM_003060.4:c.506G>C