Canonical Allele Identifier: PA2825113778
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2747532
ClinVar RCV Id: RCV003587638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1899Met
CA389034671
NM_000257.4:c.5695G>A