Canonical Allele Identifier: PA658808650
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 502729
ClinVar RCV Id: RCV000592211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Met8767Ile
CA366088780
NM_182961.4:c.26301G>T
CA366088782
NM_182961.4:c.26301G>C
CA366088784
NM_182961.4:c.26301G>A