Canonical Allele Identifier: PA2580401625
Gene: RNLS HGNC NCBI
ClinVar RCV:
RCV004180360
ClinVar Variation:
2338047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060833.1:p.Ala70Val
CA5590566
NM_018363.4:c.209C>T