Canonical Allele Identifier: PA2826845833
Gene: SYNE4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2247858
ClinVar RCV Id: RCV004104773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284664.1:p.Gly170Ser
CA405431419
NM_001297735.3:c.508G>A