Canonical Allele Identifier: PA1139680973
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 928284
ClinVar RCV Id: RCV001192060 RCV001863046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Ala1421Val
CA394857277
NM_001040114.2:c.4262C>T
CA1139664533
NM_001040114.2:c.4262_4263delinsTG