Canonical Allele Identifier: PA2829690201
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 972400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Asn1313Asp
CA1395867
NM_007123.6:c.3937A>G