Canonical Allele Identifier: PA129924
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 35483
ClinVar RCV Id: RCV000029155 RCV000657889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123910.1:p.Gln2202del
CA129923
NM_001130438.3:c.6605_6607del