Canonical Allele Identifier: PA1139710340
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 838994
ClinVar RCV Id: RCV001040656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Glu120Lys
CA7122877
NM_006177.5:c.358G>A