Canonical Allele Identifier: PA2580567970
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2217063
ClinVar RCV Id: RCV002682652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Thr3635Ser
CA344833287
NM_206933.4:c.10904C>G
CA344833302
NM_206933.4:c.10903A>T