Allele Registry

Canonical Allele Identifier: PA2825630352

Gene: SMARCAL1 HGNC NCBI

ClinVar RCV:

RCV000590927

ClinVar Variation:

496639

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120679.1:p.Gly857Glu	CA350504978 NM_001127207.2:c.2570G>A