Allele Registry

Canonical Allele Identifier: PA110341

Gene: SLC16A2 HGNC NCBI

ClinVar RCV:

RCV000012404

ClinVar Variation:

11638

HGVS (amino-acid)	Matching Registered Transcripts
NP_006508.2:p.Leu494Pro	CA341126 NM_006517.5:c.1481T>C