Allele Registry

Canonical Allele Identifier: PA2826994218

Gene: SPRY2 HGNC NCBI

ClinVar RCV:

RCV004096123

ClinVar Variation:

2233561

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305466.1:p.Gln37Pro	CA388459878 NM_001318537.1:c.110A>C