Canonical Allele Identifier: PA2830090005
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1415617
ClinVar RCV Id: RCV001933173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149062.2:p.Phe8736Leu
CA366088545
NM_033071.5:c.26208C>A
CA366088547
NM_033071.5:c.26208C>G
CA366088558
NM_033071.5:c.26206T>C