Canonical Allele Identifier: PA2580286334
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 1915622
ClinVar RCV Id: RCV002601625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Gly253Arg
CA347232877
NM_003124.5:c.757G>A
CA347232878
NM_003124.5:c.757G>C