Canonical Allele Identifier: PA645486536
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313571
ClinVar RCV Id: RCV000372793 RCV000695032 RCV001723898 RCV004021589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Val4124Leu
CA7222098
NM_182914.2:c.12370G>T
CA389953277
NM_182914.2:c.12370G>C