Canonical Allele Identifier: PA2573316699
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1515220
ClinVar RCV Id: RCV002020930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Val4255Met
CA344849260
NM_206933.4:c.12763G>A