Canonical Allele Identifier: PA2828572480
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2502048
ClinVar RCV Id: RCV003228467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362239.1:p.Lys1858Glu
CA375077315
NM_001375310.1:c.5572A>G