Canonical Allele Identifier: PA182581
Gene: USH1G HGNC NCBI

Linked Data

ClinVar Variation Id: 178570
ClinVar RCV Id: RCV000155318 RCV000725682 RCV000999863 RCV004544436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775748.2:p.Asp279Glu
CA182580
NM_173477.5:c.837C>G
CA400963030
NM_173477.5:c.837C>A