Canonical Allele Identifier: PA658801049
Gene: SYNE4 HGNC NCBI

Linked Data

ClinVar Variation Id: 517527
ClinVar RCV Id: RCV000615818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034965.1:p.His314Tyr
CA307814560
NM_001039876.3:c.940C>T