Canonical Allele Identifier: PA2825393651
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070978
ClinVar RCV Id: RCV004014480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Ser1900Thr
CA7921168
NM_001040113.2:c.5698T>A