Canonical Allele Identifier: PA2828113695
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 966208
ClinVar RCV Id: RCV001240830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350694.1:p.Gln2281Leu
CA375098602
NM_001363765.2:c.6842A>T