Canonical Allele Identifier: PA2829808260
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283619
ClinVar RCV Id: RCV000326039 RCV001079812 RCV004021140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Leu3105Phe
CA7221251
NM_015180.5:c.9315A>C
CA389977928
NM_015180.5:c.9315A>T