Canonical Allele Identifier: PA2829806644
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Leu140Val
CA7219109
NM_015180.5:c.418C>G