Allele Registry

Canonical Allele Identifier: PA108651

Gene: SPR HGNC NCBI

ClinVar RCV:

RCV000013804

RCV000498846

RCV000803472

RCV003944820

ClinVar Variation:

12941

HGVS (amino-acid)	Matching Registered Transcripts
NP_003115.1:p.Arg150Gly	CA122793 NM_003124.5:c.448A>G