Canonical Allele Identifier: PA645486312
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313494
ClinVar RCV Id: RCV000706228 RCV001660635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Leu757Ser
CA7219646
NM_182914.2:c.2270T>C