Allele Registry

Canonical Allele Identifier: PA097942

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000529995

RCV001700199

ClinVar Variation:

454354

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Asp778Val	CA389048628 NM_000257.4:c.2333A>T