Allele Registry

Canonical Allele Identifier: PA257132

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000251625

RCV003629099

ClinVar Variation:

14134

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035202.1:p.Arg1282Leu	CA257130 NM_001040113.2:c.3845G>T