Allele Registry

Canonical Allele Identifier: PA658804590

Gene: MYO7A HGNC NCBI

ClinVar Variation Id: 505113

HGVS (amino-acid)	Matching Registered Transcripts
NP_000251.3:p.Arg920Leu	CA6197926 NM_000260.4:c.2759G>T