Canonical Allele Identifier: PA2829689858
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1396703
ClinVar RCV Id: RCV001903125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Asn1129Lys
CA1395997
NM_007123.6:c.3387T>A
CA344868860
NM_007123.6:c.3387T>G