Allele Registry

Canonical Allele Identifier: PA645414981

Gene: MYH7 HGNC NCBI

ClinVar Variation Id: 235026

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg453Leu	CA10581177 NM_000257.4:c.1358G>T