Canonical Allele Identifier: PA2829808017
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283270

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Thr2669Ala
CA7221049
NM_015180.5:c.8005A>G