Canonical Allele Identifier: PA645486634
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313646
ClinVar RCV Id: RCV000306359 RCV000767326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Asn6363Ser
CA7224321
NM_182914.2:c.19088A>G