Allele Registry

Canonical Allele Identifier: PA1139680650

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV001119523

RCV004000247

ClinVar Variation:

887027

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035203.1:p.Arg1282Gln	CA394859993 NM_001040114.2:c.3845G>A