Canonical Allele Identifier: PA2829399143
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1749344
ClinVar RCV Id: RCV002347744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Glu1912Gln
CA394846499
NM_002474.3:c.5734G>C