Canonical Allele Identifier: PA2573316312
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1443694
ClinVar RCV Id: RCV001981341
ClinVar Variation Id: 2738229
ClinVar RCV Id: RCV003562545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Val2904Leu
CA37459516
NM_206933.4:c.8710G>C
CA344851469
NM_206933.4:c.8710G>T