Canonical Allele Identifier: PA2829998780
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 318089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Lys1925Arg
CA10647069
NM_022844.3:c.5774A>G