Allele Registry

Canonical Allele Identifier: PA915958802

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000414859

ClinVar Variation:

374162

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035203.1:p.Asp1461His	CA16043500 NM_001040114.2:c.4381G>C