Allele Registry

Canonical Allele Identifier: PA212695

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000035861

RCV000243331

RCV000487455

RCV001852732

ClinVar Variation:

42968

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Glu1220del	CA013921 NM_000257.4:c.3658_3660del