Canonical Allele Identifier: PA915959044
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 419054
ClinVar RCV Id: RCV000486651 RCV001189159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Ala1970Thr
CA7921043
NM_001040114.2:c.5908G>A