Canonical Allele Identifier: PA2573285966
Gene: CEP290 HGNC NCBI

Linked Data

ClinVar Variation Id: 1380530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079390.3:p.Asn390Ser
CA241154744
NM_025114.4:c.1169A>G