Allele Registry

Canonical Allele Identifier: PA097189

Gene: NPHS1 HGNC NCBI

ClinVar RCV:

RCV000049868

ClinVar Variation:

56455

HGVS (amino-acid)	Matching Registered Transcripts
NP_004637.1:p.Trp64Ser	CA250153 NM_004646.4:c.191G>C