Allele Registry

Canonical Allele Identifier: PA180817

Gene: MYH7 HGNC NCBI

ClinVar Variation Id: 177821

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Phe468Leu	CA010692 NM_000257.4:c.1402T>C CA389050696 NM_000257.4:c.1404C>A CA389050697 NM_000257.4:c.1404C>G