Canonical Allele Identifier: PA2829995648
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3071594
ClinVar RCV Id: RCV004016088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Arg669Leu
CA7922453
NM_022844.3:c.2006G>T