Allele Registry

Canonical Allele Identifier: PA354123

Gene: NPHS2 HGNC NCBI

ClinVar RCV:

RCV000210051

ClinVar Variation:

224482

HGVS (amino-acid)	Matching Registered Transcripts
NP_055440.1:p.Pro271Leu	CA354121 NM_014625.4:c.812C>T