Canonical Allele Identifier: PA296775
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181316
ClinVar RCV Id: RCV000158751 RCV002516387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys206Arg
CA016559
NM_000257.4:c.617A>G