Canonical Allele Identifier: PA645395414
Gene: SYNE4 HGNC NCBI

Linked Data

ClinVar Variation Id: 227091
ClinVar RCV Id: RCV000221990 RCV001815252 RCV002054936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034965.1:p.Gln278His
CA9393840
NM_001039876.3:c.834G>C
CA405431520
NM_001039876.3:c.834G>T