Canonical Allele Identifier: PA658677866
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448633
ClinVar RCV Id: RCV000516240 RCV000705421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Met1719Val
CA7220413
NM_182914.2:c.5155A>G