Canonical Allele Identifier: PA2826648267
Gene: USH1G HGNC NCBI

Linked Data

ClinVar Variation Id: 48127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269418.1:p.Asp355Val
CA262040
NM_001282489.3:c.1064A>T