Canonical Allele Identifier: PA2580566718
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2337840
ClinVar RCV Id: RCV002950075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ala794Asp
CA344864917
NM_206933.4:c.2381C>A