Allele Registry

Canonical Allele Identifier: PA306521

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000182502

RCV000530492

RCV001188125

RCV002492809

ClinVar Variation:

201059

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035202.1:p.Arg1049Gln	CA306519 NM_001040113.2:c.3146G>A