Canonical Allele Identifier: PA2580568264
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2073883
ClinVar RCV Id: RCV002944176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Tyr4225Cys
CA344849969
NM_206933.4:c.12674A>G