Allele Registry

Canonical Allele Identifier: PA234942

Gene: SLC16A2 HGNC NCBI

ClinVar RCV:

RCV000153954

RCV001375983

RCV003588581

ClinVar Variation:

167691

HGVS (amino-acid)	Matching Registered Transcripts
NP_006508.2:p.Arg197His	CA234941 NM_006517.5:c.590G>A