Canonical Allele Identifier: PA2825351994
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074525
ClinVar RCV Id: RCV004014059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Arg1891Lys
CA7921175
NM_001040114.2:c.5672G>A