Canonical Allele Identifier: PA1139730189
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 860559
ClinVar RCV Id: RCV001066885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334631.1:p.Gly938Arg
CA4052595
NM_001347702.2:c.2812G>A
CA366088853
NM_001347702.2:c.2812G>C