Allele Registry

Canonical Allele Identifier: PA645427379

Gene: MYO7A HGNC NCBI

ClinVar Variation Id: 235215

HGVS (amino-acid)	Matching Registered Transcripts
NP_000251.3:p.Ser1356Cys	CA6198306 NM_000260.4:c.4066A>T