Canonical Allele Identifier: PA2829808773
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 197996
ClinVar RCV Id: RCV000179186 RCV001086536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Gln3771His
CA246452
NM_015180.5:c.11313G>C
CA389941933
NM_015180.5:c.11313G>T