Allele Registry

Canonical Allele Identifier: PA097562

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000015175

RCV000480992

RCV000546277

RCV002345244

RCV003151728

RCV003319168

RCV004532358

ClinVar Variation:

14118

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg1712Trp	CA015719 NM_000257.4:c.5134C>T