Canonical Allele Identifier: PA2828113361
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1934475
ClinVar RCV Id: RCV002638733

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350694.1:p.Glu1839Ala
CA375077337
NM_001363765.2:c.5516A>C