Allele Registry

Canonical Allele Identifier: PA2580160458

Gene: NPNT HGNC NCBI

ClinVar RCV:

RCV004075220

ClinVar Variation:

2211604

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171620.1:p.Gly546Val	CA3034542 NM_001184691.2:c.1637G>T