Canonical Allele Identifier: PA1139764046
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 943136
ClinVar RCV Id: RCV001213266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Gly2928Val
CA344851242
NM_206933.4:c.8783G>T