Allele Registry

Canonical Allele Identifier: PA645416155

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000484931

RCV001180609

RCV001851137

ClinVar Variation:

418361

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg819Trp	CA16619849 NM_000257.4:c.2455C>T