Canonical Allele Identifier: PA645486652
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 287897
ClinVar RCV Id: RCV000263614 RCV000343094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Gly6546Ser
CA7224525
NM_182914.2:c.19636G>A