Canonical Allele Identifier: PA2829810717
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313668
ClinVar RCV Id: RCV000647565 RCV004021601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Pro6824Ser
CA7224941
NM_015180.5:c.20470C>T