Canonical Allele Identifier: PA645486689
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313663
ClinVar RCV Id: RCV001057188 RCV003417990 RCV004021598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Ser6808Leu
CA7224861
NM_182914.2:c.20423C>T