Canonical Allele Identifier: PA2825392333
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1499306
ClinVar RCV Id: RCV002010572 RCV002492311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Arg658Cys
CA394869048
NM_001040113.2:c.1972C>T