Canonical Allele Identifier: PA2828575026
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1064118
ClinVar RCV Id: RCV001374045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362241.2:p.Lys1846Glu
CA375076870
NM_001375312.2:c.5536A>G