Allele Registry

Canonical Allele Identifier: PA250145

Gene: NPHS1 HGNC NCBI

ClinVar RCV:

RCV000049864

ClinVar Variation:

56451

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Gly601Arg	CA250143 NM_004646.4:c.1801G>C