Canonical Allele Identifier: PA658678072
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 470938
ClinVar RCV Id: RCV000540282 RCV000993215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Ile5011Val
CA7222963
NM_182914.2:c.15031A>G