Canonical Allele Identifier: PA2741827816
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773851
ClinVar RCV Id: RCV003528643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Arg676His
CA7922454
NM_001040114.2:c.2027G>A