Canonical Allele Identifier: PA2573211273
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1357372
ClinVar RCV Id: RCV001863800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362247.1:p.Arg1825Trp
CA375076321
NM_001375318.1:c.5473C>T