Canonical Allele Identifier: PA206681
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 212341
ClinVar RCV Id: RCV000193297 RCV000346757 RCV000291749 RCV000951589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Arg8272Gln
CA206679
NM_182961.4:c.24815G>A