Allele Registry

Canonical Allele Identifier: PA296771

Gene: MYH7 HGNC NCBI

ClinVar Variation Id: 1806336

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Ala199Thr	CA016506 NM_000257.4:c.595G>A