Canonical Allele Identifier: PA2828111366
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369237
ClinVar RCV Id: RCV001894851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350688.1:p.Lys1843Glu
CA375077021
NM_001363759.2:c.5527A>G