Canonical Allele Identifier: PA2829998695
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 201091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Thr1911Lys
CA306616
NM_022844.3:c.5732C>A