Canonical Allele Identifier: PA2826648221
Gene: USH1G HGNC NCBI

Linked Data

ClinVar Variation Id: 1120134
ClinVar RCV Id: RCV001449832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269418.1:p.Glu290Asp
CA8753918
NM_001282489.3:c.870G>T
CA400961511
NM_001282489.3:c.870G>C