Canonical Allele Identifier: PA1139765202
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 969289
ClinVar RCV Id: RCV001244596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Asn4685Asp
CA344840391
NM_206933.4:c.14053A>G