Canonical Allele Identifier: PA278688
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43292
ClinVar RCV Id: RCV000036197 RCV000594226 RCV000672711 RCV001089676 RCV002504884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg1873Gln
CA278687
NM_000260.4:c.5618G>A