Canonical Allele Identifier: PA2829807920
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 470981
ClinVar RCV Id: RCV000554851
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Gly2495Arg
CA7220947
NM_015180.5:c.7483G>A
CA389958951
NM_015180.5:c.7483G>C