Allele Registry

Canonical Allele Identifier: PA296901

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000158866

RCV000219927

ClinVar Variation:

181390

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Glu1490Asp	CA015001 NM_000257.4:c.4470G>C CA389038342 NM_000257.4:c.4470G>T