Canonical Allele Identifier: PA097475
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2324
ClinVar RCV Id: RCV000002414 RCV000173937 RCV000713713 RCV003924796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Thr6211Met
CA115482
NM_015180.5:c.18632C>T