Allele Registry

Canonical Allele Identifier: PA273193

Gene: MYH7 HGNC NCBI

ClinVar Variation Id: 164378

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Tyr386Cys	CA010299 NM_000257.4:c.1157A>G