Canonical Allele Identifier: PA2580568143
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2181788
ClinVar RCV Id: RCV002595835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Pro4006Ser
CA344827007
NM_206933.4:c.12016C>T