Canonical Allele Identifier: PA2830406487
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1415617
ClinVar RCV Id: RCV001933173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Phe8784Leu
CA366088545
NM_182961.4:c.26352C>A
CA366088547
NM_182961.4:c.26352C>G
CA366088558
NM_182961.4:c.26350T>C