Canonical Allele Identifier: PA2825690881
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1064118
ClinVar RCV Id: RCV001374045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123910.1:p.Lys1834Glu
CA375076870
NM_001130438.3:c.5500A>G