Canonical Allele Identifier: PA916029155
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 289958
ClinVar RCV Id: RCV000325861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334631.1:p.Ser914Ala
CA10606609
NM_001347702.2:c.2740T>G