Allele Registry

Canonical Allele Identifier: PA915956829

Gene: MYH7 HGNC NCBI

ClinVar Allele:

642300

ClinVar RCV:

RCV000812315

RCV004001741

ClinVar Variation:

656013

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Asp554Glu	CA029049 NM_000257.4:c.1662C>A CA389050087 NM_000257.4:c.1662C>G