Allele Registry

Canonical Allele Identifier: PA110271

Gene: SLC25A22 HGNC NCBI

ClinVar RCV:

RCV000001847

RCV001851565

RCV002508754

ClinVar Variation:

1775

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177989.1:p.Pro206Leu	CA115172 NM_001191060.2:c.617C>T