Canonical Allele Identifier: PA2829808342
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313548
ClinVar RCV Id: RCV000690437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Glu3234Gln
CA7221315
NM_015180.5:c.9700G>C