Canonical Allele Identifier: PA2827935944
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 950435
ClinVar RCV Id: RCV001222143 RCV002563027
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Tyr172Phe
CA389277925
NM_001354768.3:c.515A>T