Canonical Allele Identifier: PA916029162
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 436903
ClinVar RCV Id: RCV000500060 RCV000993178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334631.1:p.Leu936Val
CA4052596
NM_001347702.2:c.2806C>G