Allele Registry

Canonical Allele Identifier: PA645415938

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000480907

RCV001851136

ClinVar Variation:

418360

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Asp737Tyr	CA16619852 NM_000257.4:c.2209G>T