Canonical Allele Identifier: PA2829399151
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2740057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Glu1915Lys
CA7921152
NM_002474.3:c.5743G>A