Canonical Allele Identifier: PA2573205711
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1429632
ClinVar RCV Id: RCV001939033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Ser34Trp
CA389278888
NM_001354770.2:c.101C>G