Allele Registry

Canonical Allele Identifier: PA270778

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000144438

RCV000182510

RCV004019090

ClinVar Variation:

88953

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035202.1:p.Leu1271Pro	CA270776 NM_001040113.2:c.3812T>C