Canonical Allele Identifier: PA2580568234
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1901014
ClinVar RCV Id: RCV002586074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ala4160Val
CA1393458
NM_206933.4:c.12479C>T