Allele Registry

Canonical Allele Identifier: PA272496

Gene: SLC16A2 HGNC NCBI

ClinVar RCV:

RCV000147499

ClinVar Variation:

159907

HGVS (amino-acid)	Matching Registered Transcripts
NP_006508.2:p.Ala150Glu	CA272495 NM_006517.5:c.449C>A