Canonical Allele Identifier: PA2573101664
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 623723
ClinVar RCV Id: RCV000761704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Arg926Leu
CA344864058
NM_206933.4:c.2777G>T