Allele Registry

Canonical Allele Identifier: PA097996

Gene: MYH7 HGNC NCBI

ClinVar Variation Id: 407189

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Gln222Lys	CA16614501 NM_000257.4:c.664C>A