Canonical Allele Identifier: PA202962
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 197575
ClinVar RCV Id: RCV000178637 RCV000299095 RCV000402645 RCV000713683 RCV001082120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_892006.3:p.Phe2312Leu
CA202961
NM_182961.4:c.6934T>C
CA366119766
NM_182961.4:c.6936T>G
CA366119767
NM_182961.4:c.6936T>A