Canonical Allele Identifier: PA645486673
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 282661
ClinVar RCV Id: RCV000514270 RCV001079226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Ala6721Thr
CA7224740
NM_182914.2:c.20161G>A