Canonical Allele Identifier: PA2829809808
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313613
ClinVar RCV Id: RCV000793716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Val5289Met
CA7223208
NM_015180.5:c.15865G>A