Canonical Allele Identifier: PA2825393658
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773782
ClinVar RCV Id: RCV003528097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Asn1904Lys
CA394846793
NM_001040113.2:c.5712C>G
CA394846794
NM_001040113.2:c.5712C>A