Canonical Allele Identifier: PA1139679417
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 919619
ClinVar RCV Id: RCV001177898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Glu643Asp
CA394869146
NM_001040114.2:c.1929G>T
CA394869147
NM_001040114.2:c.1929G>C