Allele Registry

Canonical Allele Identifier: PA2829995650

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000148694

RCV000505700

RCV000586477

RCV000776190

RCV003917465

ClinVar Variation:

161319

HGVS (amino-acid)	Matching Registered Transcripts
NP_074035.1:p.Arg669Cys	CA211699 NM_022844.3:c.2005C>T