Canonical Allele Identifier: PA2573101701
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 167816
ClinVar RCV Id: RCV000155329 RCV000723740 RCV001273050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Asn1683Ser
CA182602
NM_206933.4:c.5048A>G