Canonical Allele Identifier: PA2829998669
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1172257
ClinVar RCV Id: RCV001525973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Arg1901Lys
CA394846723
NM_022844.3:c.5702G>A