Allele Registry

Canonical Allele Identifier: PA103439

Gene: NSDHL HGNC NCBI

ClinVar RCV:

RCV000012183

ClinVar Variation:

11430

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123237.1:p.Ala182Pro	CA255884 NM_001129765.2:c.544G>C