Canonical Allele Identifier: PA1139765195
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 813242
ClinVar RCV Id: RCV001199786

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Glu4671_Arg4675del
CA1139656542
NM_206933.4:c.14011_14025del