Canonical Allele Identifier: PA2829808493
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Gly3436Ser
CA7221476
NM_015180.5:c.10306G>A