Canonical Allele Identifier: PA2825352111
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069675
ClinVar RCV Id: RCV004008219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Ser1933Gly
CA394846234
NM_001040114.2:c.5797A>G