Canonical Allele Identifier: PA2825393635
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 843071
ClinVar RCV Id: RCV001045607 RCV002348372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Asn1883Ser
CA7921181
NM_001040113.2:c.5648A>G