Allele Registry

Canonical Allele Identifier: PA2826314569

Gene: SLC7A9 HGNC NCBI

ClinVar RCV:

RCV000965433

RCV001729760

RCV003935998

ClinVar Variation:

783828

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229965.1:p.Pro482Ser	CA9358389 NM_001243036.2:c.1444C>T