Canonical Allele Identifier: PA097491
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43003
ClinVar RCV Id: RCV000148697 RCV000758078 RCV001185537 RCV001703872 RCV002504880 RCV003333016 RCV003333012 RCV003333014 RCV003333013 RCV003333015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1420Trp
CA014718
NM_000257.4:c.4258C>T