Allele Registry

Canonical Allele Identifier: PA306466

Gene: MYH11 HGNC NCBI

ClinVar Allele:

197852

ClinVar RCV:

RCV000239107

RCV000244427

RCV000405397

RCV000656918

RCV001553753

ClinVar Variation:

201037

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035202.1:p.Val1766Ile	CA306464 NM_001040113.2:c.5296G>A