Canonical Allele Identifier: PA2828113350
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2050653
ClinVar RCV Id: RCV002922018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350694.1:p.Glu1824Gln
CA5265495
NM_001363765.2:c.5470G>C