Canonical Allele Identifier: PA1139762501
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 962670
ClinVar RCV Id: RCV001236564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Gln765Glu
CA344865219
NM_206933.4:c.2293C>G