Canonical Allele Identifier: PA645420992
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 239510
ClinVar RCV Id: RCV000732128 RCV000785106 RCV001088920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Arg210Trp
CA1709008
NM_003124.5:c.628C>T