Allele Registry

Canonical Allele Identifier: PA098396

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000158523

RCV000619837

RCV000678722

RCV002466449

ClinVar Variation:

177665

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Gly741Trp	CA012022 NM_000257.4:c.2221G>T