Canonical Allele Identifier: PA645482692
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 355860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.His5370Gln
CA4055607
NM_182961.4:c.16110C>A
CA366117234
NM_182961.4:c.16110C>G