Canonical Allele Identifier: PA645486291
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313485
ClinVar RCV Id: RCV000344743 RCV004021585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Leu140Val
CA7219109
NM_182914.2:c.418C>G