Canonical Allele Identifier: PA2741873065
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2768910
ClinVar RCV Id: RCV003590993

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362247.1:p.Lys1531Arg
CA375068398
NM_001375318.1:c.4592A>G