Canonical Allele Identifier: PA2825112774
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2008725
ClinVar RCV Id: RCV002828828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1445del
CA2580616569
NM_000257.4:c.4333_4335del