Canonical Allele Identifier: PA658678020
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 470925
ClinVar RCV Id: RCV000554298 RCV004024162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Pro4232Leu
CA7222241
NM_182914.2:c.12695C>T