Canonical Allele Identifier: PA2828102986
Gene: NPC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350617.1:p.Pro120Ser
CA254414
NM_001363688.1:c.358C>T