Canonical Allele Identifier: PA2499250059
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1047425
ClinVar RCV Id: RCV001352132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334631.1:p.Asn970Ser
CA4052575
NM_001347702.2:c.2909A>G