Allele Registry

Canonical Allele Identifier: PA2580479850

Gene: SH3BGRL3 HGNC NCBI

ClinVar RCV:

RCV004212648

ClinVar Variation:

2373606

HGVS (amino-acid)	Matching Registered Transcripts
NP_112576.1:p.Ala52Val	CA702382 NM_031286.4:c.155C>T