Allele Registry

Canonical Allele Identifier: PA103432

Gene: NSDHL HGNC NCBI

ClinVar RCV:

RCV000012179

RCV002512978

ClinVar Variation:

11426

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123237.1:p.Ala105Val	CA341090 NM_001129765.2:c.314C>T