Canonical Allele Identifier: PA2741927115
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 3028276
ClinVar RCV Id: RCV003889646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Gln124Pro
CA389279353
NM_006177.5:c.371A>C