Canonical Allele Identifier: PA2829417357
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2750418
ClinVar RCV Id: RCV003589460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003118.2:p.Val1823Ala
CA375076779
NM_003127.4:c.5468T>C