Canonical Allele Identifier: PA242589
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 195914
ClinVar RCV Id: RCV000176597 RCV001087661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Thr1079Ala
CA242588
NM_182914.2:c.3235A>G