Canonical Allele Identifier: PA2829689230
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 295437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Asn760Ser
CA1396255
NM_007123.6:c.2279A>G