Allele Registry

Canonical Allele Identifier: PA212699

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000035980

ClinVar Variation:

43085

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg1909Pro	CA016422 NM_000257.4:c.5726G>C