Canonical Allele Identifier: PA2580566804
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1800581
ClinVar RCV Id: RCV002461720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Pro1058Thr
CA344862617
NM_206933.4:c.3172C>A