Canonical Allele Identifier: PA2829807751
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313525
ClinVar RCV Id: RCV000361301 RCV001288497 RCV004021587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Pro2222Ala
CA7220740
NM_015180.5:c.6664C>G