Canonical Allele Identifier: PA2827936181
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1488193
ClinVar RCV Id: RCV001988452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Asp126Asn
CA7122812
NM_001354770.2:c.376G>A