Canonical Allele Identifier: PA2742037260
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2537569
ClinVar RCV Id: RCV003256102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Arg930Trp
CA344864037
NM_206933.4:c.2788A>T