Canonical Allele Identifier: PA2825113038
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2058201
ClinVar RCV Id: RCV002915058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1579del
CA2580087877
NM_000257.4:c.4735_4737del