Canonical Allele Identifier: PA2573247899
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1393131
ClinVar RCV Id: RCV001898161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Ser117Ile
CA7122881
NM_006177.5:c.350G>T