Allele Registry

Canonical Allele Identifier: PA207766

Gene: SLC52A2 HGNC NCBI

ClinVar Allele:

207534

ClinVar RCV:

RCV000193941

RCV002280109

RCV002336517

ClinVar Variation:

212207

HGVS (amino-acid)	Matching Registered Transcripts
NP_078807.1:p.Arg169Cys	CA207764 NM_024531.5:c.505C>T