Allele Registry

Canonical Allele Identifier: PA2829475666

Gene: SCEL HGNC NCBI

ClinVar RCV:

RCV004331897

ClinVar Variation:

2569036

HGVS (amino-acid)	Matching Registered Transcripts
NP_003834.3:p.Glu51Lys	CA7010845 NM_003843.4:c.151G>A