Allele Registry

Canonical Allele Identifier: PA296886

Gene: MYH7 HGNC NCBI

ClinVar Variation Id: 181382

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg1053Trp	CA013411 NM_000257.4:c.3157C>T