Canonical Allele Identifier: PA2829998689
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073302
ClinVar RCV Id: RCV004015316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Ala1910Val
CA394846542
NM_022844.3:c.5729C>T