Allele Registry

Canonical Allele Identifier: PA296576

Gene: MYH7 HGNC NCBI

ClinVar Variation Id: 181206

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Glu931Gly	CA013097 NM_000257.4:c.2792A>G