Canonical Allele Identifier: PA1139764750
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 990776
ClinVar RCV Id: RCV001278868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ile3909Val
CA344829857
NM_206933.4:c.11725A>G