Canonical Allele Identifier: PA2829998603
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773783
ClinVar RCV Id: RCV003528098 RCV003779319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Glu1892Lys
CA394846883
NM_022844.3:c.5674G>A