Canonical Allele Identifier: PA1139717439
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 895873
ClinVar RCV Id: RCV001138216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Leu186Val
CA347232072
NM_003124.5:c.556C>G