Canonical Allele Identifier: PA2829810698
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313665
ClinVar RCV Id: RCV000293961 RCV004021599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Arg6798Gln
CA7224870
NM_015180.5:c.20393G>A