Canonical Allele Identifier: PA206618
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 212338
ClinVar RCV Id: RCV000193259 RCV003765236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Gln5265Arg
CA206616
NM_182961.4:c.15794A>G