Allele Registry

Canonical Allele Identifier: PA222961

Gene: SLC16A2 HGNC NCBI

ClinVar RCV:

RCV000514434

RCV001087210

RCV001251643

RCV001847654

RCV002362728

RCV003905062

ClinVar Variation:

95421

HGVS (amino-acid)	Matching Registered Transcripts
NP_006508.2:p.Gln138Glu	CA222960 NM_006517.5:c.412C>G