Canonical Allele Identifier: PA645486496
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 436912
ClinVar RCV Id: RCV000501363 RCV001314145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Lys3262Arg
CA7221354
NM_182914.2:c.9785A>G