Canonical Allele Identifier: PA1139764890
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 970889
ClinVar RCV Id: RCV001246547 RCV001835272 RCV003449783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Thr4242Ala
CA37412961
NM_206933.4:c.12724A>G