Canonical Allele Identifier: PA2741868000
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2875470
ClinVar RCV Id: RCV003707239
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Val33Ala
CA389278896
NM_001354770.2:c.98T>C