Allele Registry

Canonical Allele Identifier: PA645415786

Gene: MYH7 HGNC NCBI

ClinVar Allele:

399766

ClinVar RCV:

RCV000460524

RCV001584148

ClinVar Variation:

407185

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg712Cys	CA031270 NM_000257.4:c.2134C>T