Canonical Allele Identifier: PA1139762773
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 837118
ClinVar RCV Id: RCV001038387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Trp1074Arg
CA344862522
NM_206933.4:c.3220T>C
CA344862523
NM_206933.4:c.3220T>A