Canonical Allele Identifier: PA2829417109
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2768910
ClinVar RCV Id: RCV003590993

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003118.2:p.Lys1519Arg
CA375068398
NM_003127.4:c.4556A>G