Canonical Allele Identifier: PA1139764839
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 954330
ClinVar RCV Id: RCV001226771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Lys4167Glu
CA344850776
NM_206933.4:c.12499A>G