Canonical Allele Identifier: PA2573101658
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 286632
ClinVar RCV Id: RCV000339482 RCV000371237 RCV000405347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Asn820Ser
CA1396227
NM_206933.4:c.2459A>G