Canonical Allele Identifier: PA645416569
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 427118
ClinVar RCV Id: RCV000489911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg941Pro
CA389046933
NM_000257.4:c.2822G>C