Allele Registry

Canonical Allele Identifier: PA341820

Gene: NSDHL HGNC NCBI

ClinVar RCV:

RCV000020430

ClinVar Variation:

21268

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123237.1:p.Lys232del	CA341819 NM_001129765.2:c.696_698del