Allele Registry

Canonical Allele Identifier: PA2826777878

Gene: NCSTN HGNC NCBI

ClinVar RCV:

RCV001535813

ClinVar Variation:

1179000

HGVS (amino-acid)	Matching Registered Transcripts
NP_001277113.1:p.Gly13Arg	CA343275176 NM_001290184.2:c.37G>A CA343275177 NM_001290184.2:c.37G>C