Allele Registry

Canonical Allele Identifier: PA296782

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000158759

RCV000802891

RCV003486716

ClinVar Variation:

181321

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Lys246Arg	CA016736 NM_000257.4:c.737A>G