Canonical Allele Identifier: PA2830090018
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1047425
ClinVar RCV Id: RCV001352132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149062.2:p.Asn8744Ser
CA4052575
NM_033071.5:c.26231A>G