Canonical Allele Identifier: PA2573316487
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1403889
ClinVar RCV Id: RCV001901359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Thr3586Ser
CA1393927
NM_206933.4:c.10756A>T
CA344834449
NM_206933.4:c.10757C>G