Canonical Allele Identifier: PA1139710347
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 866883
ClinVar RCV Id: RCV001075241 RCV001862847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Val126Gly
CA7122867
NM_006177.5:c.377T>G