Canonical Allele Identifier: PA2827935895
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 936258
ClinVar RCV Id: RCV001205021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Gly103Ser
CA7122891
NM_001354768.3:c.307G>A