Canonical Allele Identifier: PA2829635598
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 950435
ClinVar RCV Id: RCV001222143 RCV002563027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Tyr172Phe
CA389277925
NM_006177.5:c.515A>T