Canonical Allele Identifier: PA2827935986
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2802911
ClinVar RCV Id: RCV003669098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Leu237_Ter238insArgAlaValGlnSerThrLeuTrpCysSerGlyGlyTrpValGlyTrpLeuArgProGlyGlyGlyCysThrValLeuCysIleValThrArgAlaProSerGlyProSerHisAlaLeuTyrAspArgAlaAsnIleProLysAlaPheGlySerSerSerHisAlaArgIle
CA389275964
NM_001354768.3:c.712T>A
CA389275967
NM_001354768.3:c.712T>C