Canonical Allele Identifier: PA2825109073
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2713036
ClinVar RCV Id: RCV003586861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.His251Tyr
CA049044
NM_000257.4:c.751C>T