Canonical Allele Identifier: PA1139762827
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 867201
ClinVar RCV Id: RCV001075813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Leu1152Ser
CA344868582
NM_206933.4:c.3455T>C