Allele Registry

Canonical Allele Identifier: PA645414692

Gene: MYH7 HGNC NCBI

ClinVar Variation Id: 228920

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Thr235Ala	CA10576961 NM_000257.4:c.703A>G