Canonical Allele Identifier: PA2825112296
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773926
ClinVar RCV Id: RCV003532689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1141Trp
CA037275
NM_000257.4:c.3421C>T