Canonical Allele Identifier: PA1139679429
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 925657
ClinVar RCV Id: RCV001187740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Ala649Pro
CA394869114
NM_001040114.2:c.1945G>C