Canonical Allele Identifier: PA2825691447
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 642556
ClinVar RCV Id: RCV000796040
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123910.1:p.Ala2276Thr
CA5265919
NM_001130438.3:c.6826G>A