Canonical Allele Identifier: PA2829807440
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Met1719Val
CA7220413
NM_015180.5:c.5155A>G