Canonical Allele Identifier: PA2573102027
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1310175
ClinVar RCV Id: RCV001757243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Val874Ala
CA344864401
NM_206933.4:c.2621T>C