Canonical Allele Identifier: PA2827936031
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1426949
ClinVar RCV Id: RCV001933509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Arg66Leu
CA7122909
NM_001354769.1:c.197G>T