Canonical Allele Identifier: PA2827935978
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1719071
ClinVar RCV Id: RCV002301831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Asp231Glu
CA389276086
NM_001354768.3:c.693C>G
CA389276088
NM_001354768.3:c.693C>A