Allele Registry

Canonical Allele Identifier: PA645462213

Gene: SLX4 HGNC NCBI

ClinVar Allele:

401145

ClinVar RCV:

RCV000474038

RCV000996183

RCV001194853

RCV001336769

ClinVar Variation:

407931

HGVS (amino-acid)	Matching Registered Transcripts
NP_115820.2:p.Ile1421Phe	CA7865700 NM_032444.4:c.4261A>T