Allele Registry

Canonical Allele Identifier: PA345835

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000143920

ClinVar Variation:

155812

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Tyr287Cys	CA016907 NM_000257.4:c.860A>G