Allele Registry

Canonical Allele Identifier: PA891847283

Gene: SLC16A2 HGNC NCBI

ClinVar RCV:

RCV000693919

ClinVar Variation:

572519

HGVS (amino-acid)	Matching Registered Transcripts
NP_006508.2:p.Leu494Arg	CA413659004 NM_006517.5:c.1481T>G