Canonical Allele Identifier: PA2580401656
Gene: RNLS HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060833.1:p.Arg193Gln
CA5590443
NM_018363.4:c.578G>A