Allele Registry

Canonical Allele Identifier: PA296732

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000158715

RCV000291022

RCV000339405

RCV000344866

RCV000388944

RCV001094076

RCV001179836

RCV003320124

ClinVar Variation:

181290

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg1909Gln	CA016417 NM_000257.4:c.5726G>A