Canonical Allele Identifier: PA2499305370
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1063783
ClinVar RCV Id: RCV001373659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ala1468Gly
CA344863963
NM_206933.4:c.4403C>G