Canonical Allele Identifier: PA2826204665
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1325794
ClinVar RCV Id: RCV001785331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182461.1:p.Asp2259del
CA913184751
NM_001195532.2:c.6775_6777del