Canonical Allele Identifier: PA275078
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 195258
ClinVar RCV Id: RCV000175819 RCV001376429
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Pro51Ser
CA275077
NM_006177.5:c.151C>T