Allele Registry

Canonical Allele Identifier: PA306520

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000182502

RCV000530492

RCV001188125

RCV002492809

ClinVar Variation:

201059

HGVS (amino-acid)	Matching Registered Transcripts
NP_002465.1:p.Arg1042Gln	CA306519 NM_002474.3:c.3125G>A