Canonical Allele Identifier: PA658807822
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 538372
ClinVar RCV Id: RCV000647605 RCV003905752 RCV004025743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Arg3231Cys
CA7221313
NM_182914.2:c.9691C>T