Canonical Allele Identifier: PA2825112992
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1742195
ClinVar RCV Id: RCV002335078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1552delinsLeuLeu
CA2580087886
NM_000257.4:c.4653_4655delinsCCTCCT