Canonical Allele Identifier: PA2741927107
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2797511
ClinVar RCV Id: RCV003673250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Val59Leu
CA389281296
NM_006177.5:c.175G>T
CA389281310
NM_006177.5:c.175G>C