Canonical Allele Identifier: PA645486699
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313670
ClinVar RCV Id: RCV000401937 RCV003456393 RCV004021602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Thr6901Asn
CA7224998
NM_182914.2:c.20702C>A