Allele Registry

Canonical Allele Identifier: PA915989271

Gene: NSDHL HGNC NCBI

ClinVar Allele:

26466

ClinVar RCV:

RCV000012180

ClinVar Variation:

11427

HGVS (amino-acid)	Matching Registered Transcripts
NP_057006.1:p.Gly205Ser	CA341091 NM_015922.2:c.613G>A