Canonical Allele Identifier: PA916077006
Gene: OCEL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 781446
ClinVar RCV Id: RCV000962678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078854.1:p.Pro4Thr
CA9289254
NM_024578.2:c.10C>A