Canonical Allele Identifier: PA915981021
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306177
ClinVar RCV Id: RCV000276334 RCV000333807 RCV000363893 RCV001207535 RCV001526684 RCV001833449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg836His
CA6197856
NM_001127180.2:c.2507G>A