Allele Registry

Canonical Allele Identifier: PA2829996947

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000144438

RCV000182510

RCV004019090

ClinVar Variation:

88953

HGVS (amino-acid)	Matching Registered Transcripts
NP_074035.1:p.Leu1264Pro	CA270776 NM_022844.3:c.3791T>C