Canonical Allele Identifier: PA915959035
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 318091
ClinVar RCV Id: RCV000268264 RCV000360574 RCV001119049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Val1928Met
CA10643049
NM_001040114.2:c.5782G>A