Canonical Allele Identifier: PA2827935892
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1499516
ClinVar RCV Id: RCV002040248

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Met96Ile
CA7122892
NM_001354768.3:c.288G>A
CA389280036
NM_001354768.3:c.288G>T
CA389280037
NM_001354768.3:c.288G>C