Canonical Allele Identifier: PA2499305543
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1003276
ClinVar RCV Id: RCV001299808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Glu3928Asp
CA344829429
NM_206933.4:c.11784A>T
CA344829431
NM_206933.4:c.11784A>C