Canonical Allele Identifier: PA129899
Gene: SPR HGNC NCBI

Linked Data

ClinVar Variation Id: 31917
ClinVar RCV Id: RCV000024605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003115.1:p.Gly102Cys
CA129898
NM_003124.5:c.304G>T