Canonical Allele Identifier: PA2573101581
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 552654
ClinVar RCV Id: RCV000667953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ala3189Ser
CA1394293
NM_206933.4:c.9565G>T