Allele Registry

Canonical Allele Identifier: PA2742010837

Gene: SCEL HGNC NCBI

ClinVar RCV:

RCV004331897

ClinVar Variation:

2569036

HGVS (amino-acid)	Matching Registered Transcripts
NP_659001.2:p.Glu51Lys	CA7010845 NM_144777.3:c.151G>A