Allele Registry

Canonical Allele Identifier: PA109477

Gene: NPC2 HGNC NCBI

ClinVar RCV:

RCV000020646

RCV003398552

ClinVar Variation:

21458

HGVS (amino-acid)	Matching Registered Transcripts
NP_006423.1:p.Cys99Arg	CA342111 NM_006432.5:c.295T>C