Canonical Allele Identifier: PA915958818
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_001035203.1:p.Met1515Val
CA292313
NM_001040114.2:c.4543A>G