Canonical Allele Identifier: PA2742037281
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2538014
ClinVar RCV Id: RCV003286860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Phe1213Ser
CA344868003
NM_206933.4:c.3638T>C