Canonical Allele Identifier: PA2580568496
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2140383
ClinVar RCV Id: RCV003073682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Tyr4477Phe
CA344845263
NM_206933.4:c.13430A>T