Canonical Allele Identifier: PA2827936033
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 380387
ClinVar RCV Id: RCV000422426 RCV001248164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Pro67Ser
CA7122907
NM_001354769.1:c.199C>T