Canonical Allele Identifier: PA2828576301
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1697167
ClinVar RCV Id: RCV002267513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362242.1:p.Leu1818Val
CA375076471
NM_001375313.1:c.5452C>G