Canonical Allele Identifier: PA2573082533
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 1316028
ClinVar RCV Id: RCV001757475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Arg219Gln
CA1709016
NM_003124.5:c.656G>A