Allele Registry

Canonical Allele Identifier: PA296569

Gene: MYH7 HGNC NCBI

ClinVar Variation Id: 181202

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Glu903Lys	CA012894 NM_000257.4:c.2707G>A