Canonical Allele Identifier: PA2580135636
Gene: SYNE4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2247858
ClinVar RCV Id: RCV004104773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034965.1:p.Gly283Ser
CA405431419
NM_001039876.3:c.847G>A