Canonical Allele Identifier: PA2827936058
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1042538
ClinVar RCV Id: RCV001346507 RCV004036492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Gly122Arg
CA7122874
NM_001354769.1:c.364G>A
CA389279402
NM_001354769.1:c.364G>C