Allele Registry

Canonical Allele Identifier: PA915957503

Gene: MYH7 HGNC NCBI

ClinVar Variation Id: 662104

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Ala1672Thr	CA044783 NM_000257.4:c.5014G>A