Canonical Allele Identifier: PA2827935861
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 14042
ClinVar RCV Id: RCV000015086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Ser50Thr
CA257070
NM_001354768.3:c.148T>A