Canonical Allele Identifier: PA2828113360
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1401418
ClinVar RCV Id: RCV001911799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350694.1:p.Glu1839Gly
CA375077338
NM_001363765.2:c.5516A>G