Canonical Allele Identifier: PA645449665
Gene: USH1C HGNC NCBI

Linked Data

ClinVar Variation Id: 229606
ClinVar RCV Id: RCV000218913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_710142.1:p.Pro860Leu
CA10576842
NM_153676.4:c.2579C>T