Allele Registry

Canonical Allele Identifier: PA2829399087

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV003528098

RCV003779319

ClinVar Variation:

2773783

HGVS (amino-acid)	Matching Registered Transcripts
NP_002465.1:p.Glu1892Lys	CA394846883 NM_002474.3:c.5674G>A