Canonical Allele Identifier: PA2827936037
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 884209
ClinVar RCV Id: RCV001115180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Ala76Gly
CA389280814
NM_001354769.1:c.227C>G