Canonical Allele Identifier: PA2573316576
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1500956
ClinVar RCV Id: RCV002017101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Tyr3938His
CA1393616
NM_206933.4:c.11812T>C