Canonical Allele Identifier: PA155534
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 130472
ClinVar RCV Id: RCV000118512 RCV001854571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Pro4473Ser
CA155533
NM_182914.2:c.13417C>T