Canonical Allele Identifier: PA2825108347
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791793
ClinVar RCV Id: RCV002450615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val37Ile
CA389053880
NM_000257.4:c.109G>A