Canonical Allele Identifier: PA296784
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg249Gly
CA016774
NM_000257.4:c.745C>G