Canonical Allele Identifier: PA1139675076
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 842087
ClinVar RCV Id: RCV001044438 RCV001525767 RCV002339223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1588His
CA389037680
NM_000257.4:c.4763G>A