Canonical Allele Identifier: PA145519
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Leu3892Ser
CA145517
NM_182961.4:c.11675T>C