Canonical Allele Identifier: PA2827935914
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 882488
ClinVar RCV Id: RCV001112198 RCV001314554 RCV002480481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Ala136Val
CA7122839
NM_001354768.3:c.407C>T