Canonical Allele Identifier: PA2825690815
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 959420
ClinVar RCV Id: RCV001232772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123910.1:p.Gly1793Ser
CA5265448
NM_001130438.3:c.5377G>A