Canonical Allele Identifier: PA2829417374
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369237
ClinVar RCV Id: RCV001894851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003118.2:p.Lys1838Glu
CA375077021
NM_003127.4:c.5512A>G