Canonical Allele Identifier: PA1139764675
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 48368
ClinVar RCV Id: RCV000041689 RCV000727022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Asn3742Ser
CA143249
NM_206933.4:c.11225A>G