Canonical Allele Identifier: PA645486695
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313667
ClinVar RCV Id: RCV001065859 RCV004021600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Gly6842Arg
CA7224935
NM_182914.2:c.20524G>C