Canonical Allele Identifier: PA645486470
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283270
ClinVar RCV Id: RCV000278739 RCV000700108 RCV004021127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Thr2669Ala
CA7221049
NM_182914.2:c.8005A>G