Allele Registry

Canonical Allele Identifier: PA2826778473

Gene: NCSTN HGNC NCBI

ClinVar RCV:

RCV001535813

ClinVar Variation:

1179000

HGVS (amino-acid)	Matching Registered Transcripts
NP_001277115.1:p.Gly33Arg	CA343275176 NM_001290186.2:c.97G>A CA343275177 NM_001290186.2:c.97G>C