Allele Registry

Canonical Allele Identifier: PA1139764723

Gene: USH2A HGNC NCBI

ClinVar Variation Id: 178576

HGVS (amino-acid)	Matching Registered Transcripts
NP_996816.3:p.Ala3866Val	CA182592 NM_206933.4:c.11597C>T