Canonical Allele Identifier: PA1139710231
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 916413
ClinVar RCV Id: RCV001172074 RCV003890340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Pro51Leu
CA389281570
NM_006177.5:c.152C>T