Canonical Allele Identifier: PA180705
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177753
ClinVar RCV Id: RCV000658686 RCV000628877 RCV001170267 RCV002321635 RCV001537864 RCV004528886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1045Cys
CA013367
NM_000257.4:c.3133C>T