Canonical Allele Identifier: PA1139764828
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 48399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Trp4149Arg
CA143290
NM_206933.4:c.12445T>C
CA344850887
NM_206933.4:c.12445T>A