Canonical Allele Identifier: PA915957193
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 656341
ClinVar RCV Id: RCV000812736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1066Met
CA389045228
NM_000257.4:c.3198C>G