Canonical Allele Identifier: PA2827402657
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1951873
ClinVar RCV Id: RCV002695147

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334631.1:p.Leu601Phe
CA4052870
NM_001347702.2:c.1801C>T