Allele Registry

Canonical Allele Identifier: PA645416392

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000472927

ClinVar Variation:

407172

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Val878Ala	CA16614088 NM_000257.4:c.2633T>C