Canonical Allele Identifier: PA2828111335
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1806674
ClinVar RCV Id: RCV002474103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350688.1:p.Arg1799Gln
CA375075956
NM_001363759.2:c.5396G>A