Allele Registry

Canonical Allele Identifier: PA306664

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000182553

RCV000455159

RCV001170345

RCV001208836

RCV002485206

ClinVar Variation:

201107

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035202.1:p.Ile408Thr	CA306662 NM_001040113.2:c.1223T>C