Canonical Allele Identifier: PA2827935899
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1025699
ClinVar RCV Id: RCV001326044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Gly112Val
CA389279566
NM_001354768.3:c.335G>T