Canonical Allele Identifier: PA915959024
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 418581
ClinVar RCV Id: RCV000478153 RCV000659929 RCV000777832 RCV001089216 RCV003235238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Val1886Ile
CA7921178
NM_001040114.2:c.5656G>A