Canonical Allele Identifier: PA2573101574
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 161858
ClinVar RCV Id: RCV000149394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Arg1946Leu
CA174920
NM_206933.4:c.5837G>T