Canonical Allele Identifier: PA2573101956
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 438003
ClinVar RCV Id: RCV000504870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Pro3836Leu
CA344834732
NM_206933.4:c.11507C>T