Allele Registry

Canonical Allele Identifier: PA891844915

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000693741

ClinVar Variation:

572375

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg787Pro	CA389048579 NM_000257.4:c.2360G>C