Canonical Allele Identifier: PA645483081
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 283021
ClinVar RCV Id: RCV000311509 RCV000398198 RCV000394511 RCV000647663 RCV000725192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.His8239Gln
CA4053093
NM_182961.4:c.24717C>G
CA366085395
NM_182961.4:c.24717C>A