Allele Registry

Canonical Allele Identifier: PA915989259

Gene: NSDHL HGNC NCBI

ClinVar RCV:

RCV000012179

RCV002512978

ClinVar Variation:

11426

HGVS (amino-acid)	Matching Registered Transcripts
NP_057006.1:p.Ala105Val	CA341090 NM_015922.2:c.314C>T