Allele Registry

Canonical Allele Identifier: PA2580407485

Gene: SS18L2 HGNC NCBI

ClinVar RCV:

RCV004238549

ClinVar Variation:

2400737

HGVS (amino-acid)	Matching Registered Transcripts
NP_057389.1:p.Glu37Lys	CA2335141 NM_016305.4:c.109G>A