Canonical Allele Identifier: PA1139682099
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 922990
ClinVar RCV Id: RCV001183371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Leu1858Val
CA394847431
NM_001040114.2:c.5572C>G