Allele Registry

Canonical Allele Identifier: PA2825109021

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV003586820

ClinVar Variation:

2710963

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Ile248Val	CA389052140 NM_000257.4:c.742A>G