Allele Registry

Canonical Allele Identifier: PA1139682291

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV001180707

RCV001875997

ClinVar Variation:

921354

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035203.1:p.Arg1926His	CA394846333 NM_001040114.2:c.5777G>A