Allele Registry

Canonical Allele Identifier: PA108660

Gene: SPR HGNC NCBI

ClinVar RCV:

RCV000013806

ClinVar Variation:

12943

HGVS (amino-acid)	Matching Registered Transcripts
NP_003115.1:p.Pro163Leu	CA122794 NM_003124.5:c.488C>T