Canonical Allele Identifier: PA645486290
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Asp118Val
CA7219088
NM_182914.2:c.353A>T