Canonical Allele Identifier: PA2499236134
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1172257
ClinVar RCV Id: RCV001525973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Arg1908Lys
CA394846723
NM_001040114.2:c.5723G>A