Canonical Allele Identifier: PA2825352061
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073302
ClinVar RCV Id: RCV004015316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Ala1917Val
CA394846542
NM_001040114.2:c.5750C>T