Allele Registry

Canonical Allele Identifier: PA2825109018

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV003022862

ClinVar Variation:

2099154

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Phe247Ser	CA389052143 NM_000257.4:c.740T>C