Canonical Allele Identifier: PA1139764049
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 930061
ClinVar RCV Id: RCV001195479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ser2934Thr
CA344851155
NM_206933.4:c.8801G>C