Canonical Allele Identifier: PA645486465
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376965
ClinVar RCV Id: RCV000706415 RCV004022265 RCV000436161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Val2588Met
CA7221014
NM_182914.2:c.7762G>A