Canonical Allele Identifier: PA916029167
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 502164
ClinVar RCV Id: RCV000595658 RCV000765872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334631.1:p.Thr969Met
CA4052577
NM_001347702.2:c.2906C>T