Canonical Allele Identifier: PA2830088639
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2045439
ClinVar RCV Id: RCV002918185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149062.2:p.Gln7388His
CA366099493
NM_033071.5:c.22164G>T
CA366099494
NM_033071.5:c.22164G>C