Allele Registry

Canonical Allele Identifier: PA645416976

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000412792

ClinVar Variation:

372604

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.His1331Asp	CA16042848 NM_000257.4:c.3991C>G