Canonical Allele Identifier: PA2827935869
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2794346
ClinVar RCV Id: RCV003672785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Gly57Asp
CA389281383
NM_001354768.3:c.170G>A