Canonical Allele Identifier: PA891844974
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 579335
ClinVar RCV Id: RCV000702588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1558Ser
CA257810745
NM_000257.4:c.4673T>G