Canonical Allele Identifier: PA306612
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 201089
ClinVar RCV Id: RCV000182534 RCV000280640 RCV000776147 RCV001085094 RCV001374829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Arg1869His
CA306610
NM_001040113.2:c.5606G>A