Canonical Allele Identifier: PA113529
Gene: OTOG HGNC NCBI

Linked Data

ClinVar Variation Id: 39818
ClinVar RCV Id: RCV000033039
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264198.1:p.Pro2116Leu
CA130587
NM_001277269.2:c.6347C>T