Canonical Allele Identifier: PA239989
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 194148
ClinVar RCV Id: RCV000174437 RCV000871390 RCV001697204 RCV002517677 RCV004539613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Ala7827Gly
CA239987
NM_182961.4:c.23480C>G