Canonical Allele Identifier: PA645486499
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 282107
ClinVar RCV Id: RCV000393944 RCV000532586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.His3309Leu
CA7221378
NM_182914.2:c.9926A>T