Canonical Allele Identifier: PA306611
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_002465.1:p.Arg1862His
CA306610
NM_002474.3:c.5585G>A