Allele Registry

Canonical Allele Identifier: PA2828405719

Gene: SS18L2 HGNC NCBI

ClinVar RCV:

RCV004238549

ClinVar Variation:

2400737

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357229.1:p.Glu37Lys	CA2335141 NM_001370300.1:c.109G>A