Canonical Allele Identifier: PA2825392334
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773852
ClinVar RCV Id: RCV003528644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Arg658His
CA394869047
NM_001040113.2:c.1973G>A