Canonical Allele Identifier: PA645486571
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 281790
ClinVar RCV Id: RCV000344544 RCV000559161 RCV000859415 RCV003967704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Phe4843Tyr
CA7222812
NM_182914.2:c.14528T>A