Allele Registry

Canonical Allele Identifier: PA915956679

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000807905

RCV002345822

ClinVar Variation:

652367

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg403Pro	CA389051121 NM_000257.4:c.1208G>C