Canonical Allele Identifier: PA2828111638
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1325794
ClinVar RCV Id: RCV001785331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350688.1:p.Asp2305del
CA913184751
NM_001363759.2:c.6913_6915del