Allele Registry

Canonical Allele Identifier: PA645510111

Gene: MYO7A HGNC NCBI

ClinVar Allele:

431768

ClinVar RCV:

RCV000504907

RCV001857218

ClinVar Variation:

438179

HGVS (amino-acid)	Matching Registered Transcripts
NP_000251.3:p.Thr2184Met	CA381938356 NM_000260.4:c.6551C>T