Allele Registry

Canonical Allele Identifier: PA110314

Gene: SLC16A2 HGNC NCBI

ClinVar RCV:

RCV000012405

ClinVar Variation:

11639

HGVS (amino-acid)	Matching Registered Transcripts
NP_006508.2:p.Leu360Trp	CA341127 NM_006517.5:c.1079T>G