Canonical Allele Identifier: PA2573205721
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1348715
ClinVar RCV Id: RCV002050903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Gly81Arg
CA389277487
NM_001354770.2:c.241G>A
CA389277494
NM_001354770.2:c.241G>C