Canonical Allele Identifier: PA108028
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 14042
ClinVar RCV Id: RCV000015086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Ser50Thr
CA257070
NM_006177.5:c.148T>A