Canonical Allele Identifier: PA2829417385
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2502048
ClinVar RCV Id: RCV003228467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003118.2:p.Lys1853Glu
CA375077315
NM_003127.4:c.5557A>G