Canonical Allele Identifier: PA344673
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1404Met
CA014652
NM_000257.4:c.4210G>A