Canonical Allele Identifier: PA2580139038
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1749344
ClinVar RCV Id: RCV002347744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Glu1919Gln
CA394846499
NM_001040114.2:c.5755G>C