Canonical Allele Identifier: PA116842
Gene: CLRN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243748.1:p.Cys40Gly
CA116839
NM_001256819.2:c.118T>G