Canonical Allele Identifier: PA913200051
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 618737
ClinVar RCV Id: RCV000757518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Arg693Thr
CA394868724
NM_001040113.2:c.2078G>C