Canonical Allele Identifier: PA2499305629
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1050986
ClinVar RCV Id: RCV001358965

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Lys769Glu
CA344865158
NM_206933.4:c.2305A>G