Canonical Allele Identifier: PA658677902
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_878918.2:p.Gly2495Arg
CA7220947
NM_182914.2:c.7483G>A
CA389958951
NM_182914.2:c.7483G>C