Canonical Allele Identifier: PA645416689
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 424545
ClinVar RCV Id: RCV000484625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1066Val
CA036113
NM_000257.4:c.3196A>G