Canonical Allele Identifier: PA2825690877
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2750418
ClinVar RCV Id: RCV003589460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123910.1:p.Val1828Ala
CA375076779
NM_001130438.3:c.5483T>C