Allele Registry

Canonical Allele Identifier: PA915980888

Gene: MYO7A HGNC NCBI

ClinVar RCV:

RCV001347350

ClinVar Variation:

179146

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120652.1:p.Cys635Arg	CA183808 NM_001127180.2:c.1903T>C