Canonical Allele Identifier: PA2829417334
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1167079
ClinVar RCV Id: RCV001515989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003118.2:p.Arg1803Lys
CA375076167
NM_003127.4:c.5408G>A