Allele Registry

Canonical Allele Identifier: PA645415830

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000473139

RCV000486340

ClinVar Variation:

407165

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Phe718Cys	CA16614412 NM_000257.4:c.2153T>G