Canonical Allele Identifier: PA104953
Gene: USH1G HGNC NCBI

Linked Data

ClinVar Variation Id: 48127
ClinVar RCV Id: RCV000041415 RCV001382883 RCV001799509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775748.2:p.Asp458Val
CA262040
NM_173477.5:c.1373A>T