Canonical Allele Identifier: PA915958479
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 566668
ClinVar RCV Id: RCV000686542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Pro680Ala
CA394868902
NM_001040114.2:c.2038C>G