Canonical Allele Identifier: PA2830089947
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1807208
ClinVar RCV Id: RCV002475165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149062.2:p.Thr8672Ser
CA4052617
NM_033071.5:c.26014A>T