Canonical Allele Identifier: PA916013265
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 807100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.His125Gln
CA7122869
NM_006177.5:c.375C>G
CA389279319
NM_006177.5:c.375C>A