Canonical Allele Identifier: PA2829810399
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Asn6363Ser
CA7224321
NM_015180.5:c.19088A>G