Canonical Allele Identifier: PA2829807401
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 281151
ClinVar RCV Id: RCV000340242 RCV000812641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Ala1665Val
CA7220363
NM_015180.5:c.4994C>T