Canonical Allele Identifier: PA2829808462
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 470909
ClinVar RCV Id: RCV000557826 RCV003392399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055995.4:p.Leu3406Phe
CA7221464
NM_015180.5:c.10218G>T
CA389990799
NM_015180.5:c.10218G>C