Allele Registry

Canonical Allele Identifier: PA2499284845

Gene: RNLS HGNC NCBI

ClinVar RCV:

RCV001655053

RCV001789711

ClinVar Variation:

1250700

HGVS (amino-acid)	Matching Registered Transcripts
NP_060833.1:p.Glu37Asp	CA5590594 NM_018363.4:c.111G>C CA377792133 NM_018363.4:c.111G>T