Canonical Allele Identifier: PA2825113130
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3010659
ClinVar RCV Id: RCV003862298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met1625Arg
CA389037453
NM_000257.4:c.4874T>G