Canonical Allele Identifier: PA2828112741
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 425464
ClinVar RCV Id: RCV000488052 RCV000703342 RCV001809443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350694.1:p.Thr916Ala
CA16621875
NM_001363765.2:c.2746A>G