Allele Registry

Canonical Allele Identifier: PA2829996975

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV001119523

RCV004000247

ClinVar Variation:

887027

HGVS (amino-acid)	Matching Registered Transcripts
NP_074035.1:p.Arg1275Gln	CA394859993 NM_022844.3:c.3824G>A