Canonical Allele Identifier: PA2829998759
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 924178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Glu1920Lys
CA7921149
NM_022844.3:c.5758G>A