Canonical Allele Identifier: PA645486565
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313598
ClinVar RCV Id: RCV000365286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Val4735Ile
CA7222716
NM_182914.2:c.14203G>A