Canonical Allele Identifier: PA2573316373
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1375014
ClinVar RCV Id: RCV001879451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Trp3150Arg
CA344825069
NM_206933.4:c.9448T>A
CA344825072
NM_206933.4:c.9448T>C