Canonical Allele Identifier: PA1139764826
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 813109
ClinVar RCV Id: RCV001199574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Cys4140Gly
CA344850970
NM_206933.4:c.12418T>G