Canonical Allele Identifier: PA2573247889
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1426949
ClinVar RCV Id: RCV001933509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Arg66Leu
CA7122909
NM_006177.5:c.197G>T