Canonical Allele Identifier: PA2580135631
Gene: SYNE4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2385081
ClinVar RCV Id: RCV004219925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034965.1:p.Val271Ala
CA9393849
NM_001039876.3:c.812T>C