Canonical Allele Identifier: PA645482781
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 284767
ClinVar RCV Id: RCV000725524 RCV001071366 RCV001157766 RCV001157765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Arg6065Trp
CA4055038
NM_182961.4:c.18193C>T