Canonical Allele Identifier: PA2830089960
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 289958
ClinVar RCV Id: RCV000325861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149062.2:p.Ser8688Ala
CA10606609
NM_033071.5:c.26062T>G