Allele Registry

Canonical Allele Identifier: PA117726

Gene: SLC7A9 HGNC NCBI

ClinVar Allele:

20822

ClinVar RCV:

RCV000006139

ClinVar Variation:

5783

HGVS (amino-acid)	Matching Registered Transcripts
NP_055085.1:p.Gly195Arg	CA117725 NM_014270.5:c.583G>A CA405202749 NM_014270.5:c.583G>C