Allele Registry

Canonical Allele Identifier: PA097626

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000015158

RCV000158787

RCV000456661

RCV000515361

RCV000621657

RCV001170740

ClinVar Variation:

14102

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg403Trp	CA010360 NM_000257.4:c.1207C>T