Canonical Allele Identifier: PA2742037428
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2662477
ClinVar RCV Id: RCV003443972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ala3680Val
CA37429040
NM_206933.4:c.11039C>T