Canonical Allele Identifier: PA2829995641
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 263472
ClinVar RCV Id: RCV001190249 RCV001312487 RCV003409381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Thr667Met
CA7922457
NM_022844.3:c.2000C>T