Canonical Allele Identifier: PA2829689510
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3010915
ClinVar RCV Id: RCV003862554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Arg930Ser
CA344864031
NM_007123.6:c.2790G>T
CA344864032
NM_007123.6:c.2790G>C