Canonical Allele Identifier: PA2573227898
Gene: SPR HGNC NCBI
ClinVar RCV:
RCV001902797
ClinVar Variation:
1385110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Gln49Glu
CA347230604
NM_003124.5:c.145C>G