Canonical Allele Identifier: PA2825349657
Gene: RNLS HGNC NCBI
ClinVar RCV:
RCV004121753
ClinVar Variation:
2261738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026879.2:p.Arg193Gln
CA5590443
NM_001031709.3:c.578G>A