Allele Registry

Canonical Allele Identifier: PA916075679

Gene: SLC16A12 HGNC NCBI

ClinVar RCV:

RCV000841206

ClinVar Variation:

681342

HGVS (amino-acid)	Matching Registered Transcripts
NP_998771.3:p.Trp17Gly	CA5595625 NM_213606.4:c.49T>G