Canonical Allele Identifier: PA2580139015
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1748399
ClinVar RCV Id: RCV002344728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Asp1867Gly
CA394847323
NM_001040114.2:c.5600A>G