Allele Registry

Canonical Allele Identifier: PA278721

Gene: MYO7A HGNC NCBI

ClinVar Allele:

176880

ClinVar RCV:

RCV000151482

RCV000498129

RCV001252672

RCV001291467

RCV001810427

RCV004528877

ClinVar Variation:

164664

HGVS (amino-acid)	Matching Registered Transcripts
NP_000251.3:p.Leu326Gln	CA278720 NM_000260.4:c.977T>A