Allele Registry

Canonical Allele Identifier: PA1139726787

Gene: SLC7A9 HGNC NCBI

ClinVar Variation Id: 889688

HGVS (amino-acid)	Matching Registered Transcripts
NP_055085.1:p.Tyr457His	CA9358429 NM_014270.5:c.1369T>C