Canonical Allele Identifier: PA1139764045
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 846165
ClinVar RCV Id: RCV001049404 RCV001073507 RCV001832460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Thr2920Ala
CA1394516
NM_206933.4:c.8758A>G