Canonical Allele Identifier: PA658677961
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448620
ClinVar RCV Id: RCV000516246 RCV000647581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Gly3436Ser
CA7221476
NM_182914.2:c.10306G>A