Canonical Allele Identifier: PA2829998602
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 138358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Glu1892Asp
CA292332
NM_022844.3:c.5676G>C
CA394846869
NM_022844.3:c.5676G>T