Canonical Allele Identifier: PA2829399032
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1997289
ClinVar RCV Id: RCV002791681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Asp1860Tyr
CA394847329
NM_002474.3:c.5578G>T