Canonical Allele Identifier: PA915981059
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229004
ClinVar RCV Id: RCV000216662 RCV000488266 RCV001112846 RCV001112847 RCV001112848 RCV001276696 RCV001375364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg933His
CA6197936
NM_001127180.2:c.2798G>A