Canonical Allele Identifier: PA2827936026
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2797511
ClinVar RCV Id: RCV003673250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Val59Leu
CA389281296
NM_001354769.1:c.175G>T
CA389281310
NM_001354769.1:c.175G>C