Allele Registry

Canonical Allele Identifier: PA658804446

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000628983

ClinVar Variation:

525016

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Val606Leu	CA389049756 NM_000257.4:c.1816G>T CA389049757 NM_000257.4:c.1816G>C