Canonical Allele Identifier: PA2829998687
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1468105
ClinVar RCV Id: RCV001970582 RCV004044639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Ala1910Thr
CA7921156
NM_022844.3:c.5728G>A