Canonical Allele Identifier: PA2827936139
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2802911
ClinVar RCV Id: RCV003669098
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Leu237_Ter238insArgAlaValGlnSerThrLeuTrpCysSerGlyGlyTrpValGlyTrpLeuArgProGlyGlyGlyCysThrValLeuCysIleValThrArgAlaProSerGlyProSerHisAlaLeuTyrAspArgAlaAsnIleProLysAlaPheGlySerSerSerHisAlaArgIle
CA389275964
NM_001354769.1:c.712T>A
CA389275967
NM_001354769.1:c.712T>C