Canonical Allele Identifier: PA184443
Gene: USH1G HGNC NCBI

Linked Data

ClinVar Variation Id: 179451
ClinVar RCV Id: RCV000156240 RCV001517890 RCV003389459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775748.2:p.Lys239Asn
CA184442
NM_173477.5:c.717G>C
CA400963706
NM_173477.5:c.717G>T