Canonical Allele Identifier: PA2573101798
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 595855
ClinVar RCV Id: RCV000731521 RCV003453530 RCV003453529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Arg3744Gly
CA344822374
NM_206933.4:c.11230A>G