Canonical Allele Identifier: PA2830421936
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_878914.1:p.Ala243Thr
CA7224740
NM_182910.2:c.727G>A