Canonical Allele Identifier: PA1139682243
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 927693
ClinVar RCV Id: RCV001191153 RCV001240359 RCV002484046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Arg1912Gln
CA394846654
NM_001040114.2:c.5735G>A