Canonical Allele Identifier: PA2580236943
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1934475
ClinVar RCV Id: RCV002638733

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362247.1:p.Glu1871Ala
CA375077337
NM_001375318.1:c.5612A>C