Canonical Allele Identifier: PA2827936019
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 195258
ClinVar RCV Id: RCV000175819 RCV001376429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Pro51Ser
CA275077
NM_001354769.1:c.151C>T