Canonical Allele Identifier: PA2580139012
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2089350
ClinVar RCV Id: RCV003005506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Ser1850Thr
CA394847527
NM_001040114.2:c.5548T>A