Canonical Allele Identifier: PA2826279478
Gene: OCLN HGNC NCBI

Linked Data

ClinVar Variation Id: 1283292
ClinVar RCV Id: RCV001696436
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001192183.1:p.Val308Leu
CA3294546
NM_001205254.2:c.922G>C
CA360066486
NM_001205254.2:c.922G>T