Allele Registry

Canonical Allele Identifier: PA2829399159

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV001180707

RCV001875997

ClinVar Variation:

921354

HGVS (amino-acid)	Matching Registered Transcripts
NP_002465.1:p.Arg1919His	CA394846333 NM_002474.3:c.5756G>A