Canonical Allele Identifier: PA2829998901
Gene: MYH11 HGNC NCBI
ClinVar RCV:
RCV001916949
ClinVar Variation:
1421510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Thr1936Ile
CA394844583
NM_022844.3:c.5807C>T