Canonical Allele Identifier: PA296784
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181322
ClinVar RCV Id: RCV000577986 RCV000578103 RCV000578064 RCV000578004 RCV001041039 RCV003320125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg249Gly
CA016774
NM_000257.4:c.745C>G