Canonical Allele Identifier: PA2829810476
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313651
ClinVar RCV Id: RCV000799529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Asp6458His
CA7224448
NM_015180.5:c.19372G>C