Canonical Allele Identifier: PA2828576546
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1254403
ClinVar RCV Id: RCV001665328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362242.1:p.Asn2279del
CA2579470529
NM_001375313.1:c.6837_6839del