Canonical Allele Identifier: PA645486626
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313638
ClinVar RCV Id: RCV000792210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Ala6078Thr
CA7224016
NM_182914.2:c.18232G>A