Canonical Allele Identifier: PA2580568273
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2202942
ClinVar RCV Id: RCV002634335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Pro4232Leu
CA344849796
NM_206933.4:c.12695C>T