Canonical Allele Identifier: PA2573227905
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 1412099
ClinVar RCV Id: RCV001943126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Lys261Arg
CA1709035
NM_003124.5:c.782A>G