Canonical Allele Identifier: PA645486386
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313509
ClinVar RCV Id: RCV000539755 RCV001288496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Tyr1638His
CA7220350
NM_182914.2:c.4912T>C