Canonical Allele Identifier: PA2828574871
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2768910
ClinVar RCV Id: RCV003590993
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362241.2:p.Lys1531Arg
CA375068398
NM_001375312.2:c.4592A>G