Canonical Allele Identifier: PA2573316629
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1468410
ClinVar RCV Id: RCV001970649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Ile4102Met
CA344851330
NM_206933.4:c.12306C>G