Canonical Allele Identifier: PA2829689306
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 374593
ClinVar RCV Id: RCV000415731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Thr806Ala
CA16043807
NM_007123.6:c.2416A>G