Allele Registry

Canonical Allele Identifier: PA2825952870

Gene: SCEL HGNC NCBI

ClinVar RCV:

RCV004331897

ClinVar Variation:

2569036

HGVS (amino-acid)	Matching Registered Transcripts
NP_001154178.1:p.Glu51Lys	CA7010845 NM_001160706.1:c.151G>A