Canonical Allele Identifier: PA2829807820
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 538336
ClinVar RCV Id: RCV000647547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Arg2365Cys
CA7220847
NM_015180.5:c.7093C>T