Canonical Allele Identifier: PA645486562
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313595
ClinVar RCV Id: RCV000304989 RCV004021593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Lys4691Glu
CA7222674
NM_182914.2:c.14071A>G