Canonical Allele Identifier: PA2573102078
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 597189
ClinVar RCV Id: RCV000733236

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Thr2939Ala
CA344851076
NM_206933.4:c.8815A>G