Allele Registry

Canonical Allele Identifier: PA645417901

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000489988

ClinVar Variation:

427207

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Glu1787Gln	CA389035733 NM_000257.4:c.5359G>C