Canonical Allele Identifier: PA2829690215
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2167757
ClinVar RCV Id: RCV003086610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Gln1321Pro
CA344867097
NM_007123.6:c.3962A>C