Allele Registry

Canonical Allele Identifier: PA645416001

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000429053

RCV001381453

ClinVar Variation:

380277

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Gly741Glu	CA16606949 NM_000257.4:c.2222G>A