Allele Registry

Canonical Allele Identifier: PA2825349617

Gene: RNLS HGNC NCBI

ClinVar RCV:

RCV001655053

RCV001789711

ClinVar Variation:

1250700

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026879.2:p.Glu37Asp	CA5590594 NM_001031709.3:c.111G>C CA377792133 NM_001031709.3:c.111G>T