Allele Registry

Canonical Allele Identifier: PA211701

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000148694

RCV000505700

RCV000586477

RCV000776190

RCV003917465

ClinVar Variation:

161319

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035202.1:p.Arg676Cys	CA211699 NM_001040113.2:c.2026C>T