Canonical Allele Identifier: PA645486577
Gene: SYNE2 HGNC NCBI

Linked Data

ClinVar Variation Id: 313602
ClinVar RCV Id: RCV000551849 RCV004021595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Phe4994Leu
CA7222952
NM_182914.2:c.14980T>C
CA389939878
NM_182914.2:c.14982T>A
CA389939879
NM_182914.2:c.14982T>G