Canonical Allele Identifier: PA645486594
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313613
ClinVar RCV Id: RCV000793716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Val5289Met
CA7223208
NM_182914.2:c.15865G>A