Allele Registry

Canonical Allele Identifier: PA097040

Gene: NPHS1 HGNC NCBI

ClinVar Allele:

71129

ClinVar RCV:

RCV000049903

RCV001853056

ClinVar Variation:

56490

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Leu96Val	CA250214 NM_004646.4:c.286C>G