Canonical Allele Identifier: PA2828113364
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 661303
ClinVar RCV Id: RCV000818691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350694.1:p.Ala1845Asp
CA375077438
NM_001363765.2:c.5534C>A