Canonical Allele Identifier: PA2826204315
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1697167
ClinVar RCV Id: RCV002267513
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182461.1:p.Leu1793Val
CA375076471
NM_001195532.2:c.5377C>G