Canonical Allele Identifier: PA2829417387
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_003118.2:p.Glu1854Gly
CA375077338
NM_003127.4:c.5561A>G