Canonical Allele Identifier: PA891849190
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 566802
ClinVar RCV Id: RCV000686715 RCV001724135 RCV001573189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Asp69Glu
CA1708913
NM_003124.5:c.207C>G
CA347230746
NM_003124.5:c.207C>A