Allele Registry

Canonical Allele Identifier: PA132238

Gene: MYO7A HGNC NCBI

ClinVar RCV:

RCV000036080

RCV000666826

RCV001112680

RCV001112681

RCV001112682

RCV001276686

RCV001852742

ClinVar Variation:

43176

HGVS (amino-acid)	Matching Registered Transcripts
NP_000251.3:p.Arg740Trp	CA132237 NM_000260.4:c.2218C>T