Canonical Allele Identifier: PA2829997587
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 138345
ClinVar RCV Id: RCV000126953 RCV000244209 RCV000471823 RCV000769663 RCV001812085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Met1508Val
CA292313
NM_022844.3:c.4522A>G