Allele Registry

Canonical Allele Identifier: PA2741828565

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV003528098

RCV003779319

ClinVar Variation:

2773783

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035203.1:p.Glu1899Lys	CA394846883 NM_001040114.2:c.5695G>A