Canonical Allele Identifier: PA1139717495
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 962681
ClinVar RCV Id: RCV001236582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Tyr259Cys
CA1709032
NM_003124.5:c.776A>G