Canonical Allele Identifier: PA645482782
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 262173
ClinVar RCV Id: RCV000248584 RCV000725762 RCV001087053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Leu6068Phe
CA4055035
NM_182961.4:c.18204G>C
CA366096967
NM_182961.4:c.18204G>T