Canonical Allele Identifier: PA2499242123
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_001192184.1:p.Val57Leu
CA3294546
NM_001205255.1:c.169G>C
CA360066486
NM_001205255.1:c.169G>T