Canonical Allele Identifier: PA2828575031
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369237
ClinVar RCV Id: RCV001894851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362241.2:p.Lys1855Glu
CA375077021
NM_001375312.2:c.5563A>G