Canonical Allele Identifier: PA658808037
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 538357
ClinVar RCV Id: RCV000647578 RCV004025742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Gln6747Pro
CA7224796
NM_182914.2:c.20240A>C