Canonical Allele Identifier: PA645486512
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Val3827Leu
CA7221782
NM_182914.2:c.11479G>C
CA389942984
NM_182914.2:c.11479G>T