Canonical Allele Identifier: PA2829417375
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2050653
ClinVar RCV Id: RCV002922018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003118.2:p.Glu1839Gln
CA5265495
NM_003127.4:c.5515G>C