Canonical Allele Identifier: PA129924
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 35483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123910.1:p.Gln2202del
CA129923
NM_001130438.3:c.6605_6607del
CA375091439
NM_001130438.3:c.6604C>T