Allele Registry

Canonical Allele Identifier: PA2826141785

Gene: NPNT HGNC NCBI

ClinVar RCV:

RCV004075220

ClinVar Variation:

2211604

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171619.1:p.Gly533Val	CA3034542 NM_001184690.2:c.1598G>T