Canonical Allele Identifier: PA2741828603
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2740057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Glu1922Lys
CA7921152
NM_001040114.2:c.5764G>A