Canonical Allele Identifier: PA2573247888
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1510220
ClinVar RCV Id: RCV002011601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Arg66Gly
CA7122912
NM_006177.5:c.196C>G