Canonical Allele Identifier: PA2827936060
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 807100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.His125Gln
CA7122869
NM_001354769.1:c.375C>G
CA389279319
NM_001354769.1:c.375C>A