Canonical Allele Identifier: PA2825690897
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 861437
ClinVar RCV Id: RCV001067960
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123910.1:p.Arg1849Gln
CA5265497
NM_001130438.3:c.5546G>A