Canonical Allele Identifier: PA2825393684
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 921354
ClinVar RCV Id: RCV001180707 RCV001875997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Arg1926His
CA394846333
NM_001040113.2:c.5777G>A