Canonical Allele Identifier: PA2829810246
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313637
ClinVar RCV Id: RCV000528583 RCV000993217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Ala6064Thr
CA7223961
NM_015180.5:c.18190G>A