Allele Registry

Canonical Allele Identifier: PA098813

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000015165

RCV001213330

ClinVar Variation:

14109

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Phe764Leu	CA012091 NM_000257.4:c.2292C>G CA389048716 NM_000257.4:c.2292C>A CA389048720 NM_000257.4:c.2290T>C