Allele Registry

Canonical Allele Identifier: PA645425097

Gene: SLC17A5 HGNC NCBI

ClinVar Allele:

236898

ClinVar RCV:

RCV000224654

RCV000327513

RCV001083032

RCV001164158

RCV004532820

ClinVar Variation:

235209

HGVS (amino-acid)	Matching Registered Transcripts
NP_036566.1:p.Val442Ile	CA3890290 NM_012434.5:c.1324G>A