Allele Registry

Canonical Allele Identifier: PA306465

Gene: MYH11 HGNC NCBI

ClinVar Allele:

197852

ClinVar RCV:

RCV000239107

RCV000244427

RCV000405397

RCV000656918

RCV001553753

ClinVar Variation:

201037

HGVS (amino-acid)	Matching Registered Transcripts
NP_002465.1:p.Val1759Ile	CA306464 NM_002474.3:c.5275G>A