Canonical Allele Identifier: PA645486596
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313614
ClinVar RCV Id: RCV000345968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Gln5376Arg
CA7223284
NM_182914.2:c.16127A>G